ClinicalTrials.gg
RecruitingNCT03945968STOPRISKUpdated Apr 4, 2025

The Role of Concomitant Diseases in Postoperative Complications Risk Stratification.

An observational study in Coronary Heart Disease, Anemia and Bronchial Asthma, sponsored by Russian Federation of Anesthesiologists and Reanimatologists. Recruiting at 38 sites in Russian Federation. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2025-04-04.

Sponsored by Russian Federation of Anesthesiologists and Reanimatologists · Observational

From the registry’s dates

  • Primary completion was expected by Dec 2025, 10 months ago, but the record still lists the study as recruiting.
  • Started Jul 2019; still recruiting 7 years 4 months later.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
16,000
Ages
18 Years and older
Sex
All
01

Study summary

Study is conducted to assess the prevalence and structure of comorbidity among patients undergoing abdominal surgery and produce the stratification of the risk of postoperative complications by identifying independent predictors for its development.

Read the detailed description

Advances in modern anesthesiology have significantly reduced the risk of anesthesia compared to the last century, however, the level of perioperative hospital mortality of planned operations at the moment is on average about 0.5% (ISOS group, 2016). Weiser et al. (2016) estimated that more than 313 million adults worldwide are subject to surgery each year. Thus, the number of deaths may result in several million each year worldwide. However, the study of the mortality risk is associated with certain difficulties, because over the past half century, this figure has decreased a hundred times and the study requires studies that include a large number of participants.

Current research focuses on other outcome criteria - postoperative complications. Thus, anesthetic risk often refers to the risk of postoperative complications. The frequency of these complications varies in a wide range, ranging from 3 to 18 % (Gawande AA, 1999, Kable AK, 2002, Malik OS, 2018). The differences in the data are explained by the lack of clear definitions and differences in the design of studies, but the fact that the development of postoperative complications increases the risk of death several times (ISOS group, 2016) can be considered undoubted. However, despite the importance of this issue, in modern literature there is no clear idea of what is considered a high risk and which of the patients corresponds to this category.

Understanding whether a patient is at high risk is an essential task - it allows you to obtain meaningful informed consent of the patient, as well as to understand whether to apply strategies for the prevention of complications (targeted infusion therapy, protective respiratory support, especially monitoring in the postoperative period, etc.).

Attempts at preoperative risk stratification have been made for many decades, some scales estimate the initial physical status (ASA scale) (Young J, 2015) and predict mortality, others estimate the risk of specific complications (Lee index, respiratory risk scale, etc.) .

Scales including intraoperative and postoperative parameters such as the POSSUM series of scales (Whiteley MS, 1996) are also being developed. The analysis shows that in routine clinical practice, these scales are not used very often, due to their limitations: subjectivity, technical complexity and often - low specificity and sensitivity.

Concomitant diseases are the strongest predictors of postoperative adverse events and annual mortality. Monk et al. (2005) demonstrated that Charlson's comorbidity score of 3 or more significantly increased the risk of death. In addition, in most clinical studies, the ASAclassification of physical status as a kind of comprehensive assessment of patient comorbidity has repeatedly proved to be one of the strongest independent predictors of postoperative morbidity and mortality, despite the fact that this assessment is based on subjective perception (Watt J., 2018).

The main concomitant diseases that are independent predictors of perioperative complications are diseases of the cardiovascular and respiratory systems (Van Diepen S, 2011). Increasing age, anemia, obesity, diabetes - these conditions also increase the risk of an adverse outcome. Diseases of the Central nervous system and neuromuscular diseases significantly disrupt the function of respiration, can change the level of the Autonomous regulation of the cardiovascular system, lead to significant cognitive disorders and nutritional deficiency, which also increases the risk of perioperative complications (Hachenberg T, 2014).

On the other hand, large-scale observational studies conducted in recent years in a number of countries have not identified comorbidities as independent predictors of postoperative complications (Malik, 2018).

Thus, data on the risk effects of comorbidities are contradictory and may be influenced by differences in the frequency and structure of these diseases in heterogeneous populations, as well as in different treatment strategies for cardiovascular, respiratory and other diseases. The identification of these risk factors is necessary to understand the pathophysiology of complications and identify potential ways to reduce anesthetic risk, such as the correction of concomitant disease.

The degree of risk of surgery, of course, depends not only on the presence of comorbidities and their combinations, but also on the severity of surgical injury (Pearse RM, 2012, ISOS group, 2017), as well as the level of exposure to drugs for anesthesia and anesthetic techniques (Malik OS, 2018), therefore, the allocation of risk groups without these factors is also not appropriate.

Objective: to assess the frequency and structure of comorbidities in patients undergoing surgery on the abdominal organs and to stratify the risk of postoperative complications by determining independent

Evaluated parameters in study:

  1. Age, gender; 2. Class of physical status by ASA; 3. The presence and type of concomitant disease; 3.1 CHD; 3.2 CHF; 3.3 Heart rhythm disorders; 3.4 COPD; 3.5 Bronchial Asthma; 3.6 CKD; 3.7 CNS diseases; 3.7.1 Stroke; 3.7.2 Epilepsy; 3.7.3 Parkinson's Disease; 3.7.4 Alzheimer's Disease; 3.8 Neuromuscular diseases; 3.9 Diabetes; 3.10 Anemia; 4 Treatment received by the patient; 4.1 β-blockers; 4.2 ACE Inhibitors; 4.3 Aldosterone antagonists; 4.4 Statins; 4.5 Anticoagulants; 4.6 Diuretics; 4.7 Bronchodilators; 4.8 Corticosteriods; 4.9 Insulin; 4.10 Anticonvulsants; 5. The type and severity of surgery ; 5.1 Open surgery on the organs of the upper abdomen; 5.2 Coloproctological operations; 5.3 Gynecological surgery; 5.4 Urological surgery; 5.5 Operations on vessels of the abdominal cavity; 5.6 Abdominal wall surgery; 5.7 Laparoscopic surgery; 6 Type of anesthesia; 6.1 Spinal; 6.2 Epidural; 6.3 Combined spinal-epidural; 6.4 Intravenous; 6.5 Combined; 6.6 General+epidural; 7. Integral scales; 7.1 The cognitive function of the Montreal scale ; 7.2 Respiratory risk ; 7.3 Lee's Cardiovascular Risk Scale ; 7.4 NSQIP Cardiac risk scale ; 7.5 Hepatic insufficiency according to MELD; 7.6 CKD Stage by Level of GFR and Albuminuria; 7.7 COPD degree by GOLD.

Order of conduct

  1. The data is registered in the Excel electronic database in a uniform format for all centers (the form will be sent by the coordinator to all centers participating in the study prior to the inclusion of patients).
  2. All centers need to get approval by the local ethics committee before the start of the study. The study protocol will be registered in Clinicaltrial.gov.
  3. The study includes all patients operated on within one operational day at the discretion of the center and meeting the inclusion criteria with registration in the questionnaire of the day of the week.
  4. All patients could sign informed consent to participate in the study prior to inclusion in the study.
  5. Before surgery, data on the patient and all studied factors specified in the study protocol are entered into the database.
  6. All patients included in the study are monitored before discharge from the hospital with registration of the data specified in the protocol.
  1. Every last day of the working week, all completed cases are sent as a separate Excel file to the study coordinator by email to trembachnv@mail.ru 7. The originals of the questionnaires are stored in the centers for the entire study time and for 3 years after its completion.
  1. The summary database is formed by the study coordinator and provided to the centers after the end of the study.

Statistical analysis The sample size was calculated taking into account the fact that at least 10 cases of postoperative complications per one factor included in the final regression model are required. Given the wide range of complication rates in previous studies (from 3% to 20%), we have chosen a lower bound for a more accurate assessment. To include 20 potential risk factors in the regression model, 200 cases of postoperative complications are required, which at a frequency of 3% is not less than 7000 people. Taking into account the risk of data loss, and taking into account as many potential risk factors as possible, the size of the required sample was increased to 12,000 people, which will also assess the contribution of comorbidities to certain groups of complications. For validation of predictive models will be recruited 4,000 additional. The inclusion of the patient in the main and validation group will be carried out randomly.

The character of distribution of studied parameters will be evaluated using the criterion Kolmogorov-Smirnov. The continuous data will be presented as the median and interquartile range for the nonparametric distribution and as the mean and standard deviation for the parametric distribution. Categorical variables will be presented as the number of patients and a percentage of the total number of patients.

For the initial assessment of the Association of the factor with postoperative complications, a single-factor analysis using the χ2 criterion and the Mann-Whitney test will be carried out. All variables with a reliable relationship identified in the univariate analysis (p less than 0.05) will be included in logistic regression if there is no collinearity between them (correlation coefficient less than 0.25). The logistic regression model will be constructed using a step-by-step reverse inclusion procedure in which the presence of a complication will be a dependent variable. Potential predictors will be removed if this exception does not cause a significant change in the log likelihood ratio. The criterion for excluding the factor will be set at the significance level of 0.05. Adjusted odds ratios and 95% confidence intervals will also be calculated.

The resulting predictive model will be evaluated in the validation group using ROC analysis and the Hosmer-Lemeshov test.

02

Conditions studied

  • Coronary Heart Disease
  • Anemia
  • Bronchial Asthma
  • Stroke
  • Epilepsy
  • Parkinson's Disease
  • Heart Rhythm Disorders
  • Alzheimer's Disease
  • Neuromuscular Diseases
  • Diabetes
  • Chronic Heart Failure
  • Chronic Obstructive Pulmonary Disease
  • Chronic Kidney Diseases

Keywords

  • anesthesia
  • concomitant diseases
  • risk stratification
03

In context

Coronary Disease

1,520 studies on the registry are indexed under Coronary Disease; 167 are open to participants now.

This study's planned enrollment of 16,000 is above the median of 916 across 478 observational studies indexed under Coronary Disease.

Browse Coronary Disease studies →

Lead sponsor

Russian Federation of Anesthesiologists and Reanimatologists is the lead sponsor of 6 studies on the registry; 3 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Probability sample

Study population

Adult atients undergoing an abdominal surgery in study centers

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • surgical interventions on the abdominal organs,
  • 1-3 class

Exclusion criteria

Exclusion Criteria:

  • the inability to assess the factors included in the study,
  • acute massive blood loss, aspiration,
  • bronchospasm,
  • anaphylactic reactions,
  • malignant hyperthermia
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

ASA physical status

The anaesthetists’ scale of health before surgery: I is healthy, II has a mild illness that is under control, III a severe one, IV a severe illness that is a constant threat to life. V and VI are used for the critically ill and for organ donors.

05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
16,000 participants (estimated)
Patient registry
No
Biospecimen retention
Samples without dna
06

What researchers measure

Primary outcomes

  1. incidence of postoperative complications

    Postoperative complications (according to the definitions of ESA-SCICM, 2015) 1. Acute kidney damage 2. ARDS 3. The failure of the anastomose 4. Arrhythmias 5. Cardiac arrest 6. Cardiogenic pulmonary edema 7. Postoperative delirium 8. Myocardial infarction 9. Pneumonia 10. Paresis of the intestine 11. Postoperative bleeding 12. Pulmonary thromboembolism 13. Stroke 14. Wound infection NSQIP complications: 1. Acute respiratory failure 2. Unplanned reintubation 3. Sepsis/septic shock 4. Wound dehiscence 5. Postoperative transfusion

    Time frame: 7 days after surgery

Secondary outcomes

  1. mortality after abdominal surgery

    30-day mortality

    Time frame: 30 days

07

Study locations

37 of 38 sites recruiting
  • The First City Clinical Hospital. n.a. E. E. Volosevich
    Arkhangel'sk, Russian Federation
    Recruiting
    • Mikhail Kirov, MD · Contact
  • Astrakhan State Medical University
    Astrakhan, Russian Federation
    Recruiting
    • Irakli Kitiashvili, MD · Contact
    • Irakli Kitiashvili, MD · Principal investigator
  • Chelyabinsk Regional Clinical Center of Oncology and Nuclear Medicine
    Chelyabinsk, Russian Federation
    Recruiting
    • Dmitry Voroshin, MD · Contact
  • South-Ural State Medical University
    Chelyabinsk, Russian Federation
    Recruiting
  • Chita state medical Academy of the Ministry of health of the Russian Federation
    Chita, Russian Federation
    Recruiting
    • Konstantin Shapovalov, MD · Contactshkg26@mail.ru
    • Konstantin Shapovalov, MD · Principal investigator
  • Ekaterinburg City clinical hospital № 40
    Ekaterinburg, Russian Federation
    Recruiting
    • Vladimir Rudnov, MD · Contactvrudnov@mail.ru
    • Vladimir Rudnov, MD · Principal investigator
  • Sverdlovsk regional clinicl hospital №1
    Ekaterinburg, Russian Federation
    Recruiting
    • Dmitry Levit, PhD · Contactd78@inbox.ru
    • Dmitry Levit, PhD · Principal investigator
  • Kazan State Medical University
    Kazan, Russian Federation
    Recruiting
    • Veronika Davydova, PhD · Contactvevojuyar@gmail.com
    • Veronika Davydova, PhD · Principal investigator
  • Republic Clinical Hospital Ministry of Health care of the Republic of Tatarstan
    Kazan, Russian Federation
    Recruiting
    • Ainagul Bayalieva, MD · Contactbayalieva1@yandex.ru
    • Ainagul Bayalieva, MD · Principal investigator
  • Research Institute for Complex Issues of Cardiovascular Diseases
    Kemerovo, 650002, Russian Federation
    Recruiting
  • Regional clinical hospital №2
    Krasnodar, 350012, Russian Federation
    Recruiting
    • Nikita Trembach, PhD · Contactnikitkax@mail.ru
    • Nikita Trembach, PhD · Principal investigator
  • Kuban State Medical University
    Krasnodar, 350063, Russian Federation
    Recruiting
    • Igor Zabolotskikh · Contactpobeda_zib@mail.ru
    • Igor Zabolotskikh, MD · Principal investigator
  • Research Institute Regional Clinical Hospital named after S.V. Ochapovsky
    Krasnodar, Russian Federation
    Recruiting
    • Yuri Malyshev, MD · Contactmalyshevyp@mail.ru
    • Yuri Malyshev, MD · Principal investigator
  • Krasnoyarsk State Medical University named after Prof. V.F.Voino-Yasenetsky
    Krasnoyarsk, 660022, Russian Federation
    Recruiting
    • Alexey Gritsan, MD · Contactgritsan67@mail.ru
    • Alexey Gritsan, MD · Principal investigator
  • Burnasyan federal medical biophysical center of federal medical biological agency
    Moscow, 123098, Russian Federation
    Recruiting
    • Sergey Voskanyan, MD · Contactvoskanyan_se@mail.ru
    • Sergey Voskanyan, MD · Principal investigator
  • City clinical hospital named after S.S. Yudin
    Moscow, Russian Federation
    Recruiting
    • Denis Protsenko, PhD · Contactdrprotsenko@me.com
    • Denis Protsenko, PhD · Principal investigator
  • City clinical hospital №1 named after N.I. Pirogov
    Moscow, Russian Federation
    Recruiting
    • Marat Magomedov, PhD · Contactmma16@bk.ru
    • Marat Magomedov, PhD · Principal investigator
  • City Clinical Hospital. n.a. F.I. Inozemtseva
    Moscow, Russian Federation
    Recruiting
    • Nina Arikan · Contact
  • FGBU "Central clinical hospital with polyclinic" of the President administration of the Russian Federation
    Moscow, Russian Federation
    Recruiting
    • Rinat Gubaidullin, MD · Contactwww.tempcor@list.ru
    • Rinat Gubaidullin, MD · Principal investigator
  • Moscow cancer research Institute named after P. A. Herzen
    Moscow, Russian Federation
    Recruiting
  • Moscow City Oncological Hospital № 62
    Moscow, Russian Federation
    Recruiting
  • Moscow regional research clinical Institute named after M. F. Vladimirsky
    Moscow, Russian Federation
    Recruiting
    • Alexey Ovezov, MD · Contactamolex@mail.ru
    • Alexey Ovezov, MD · Principal investigator
  • National Medical and Surgical Center named after N.I. Pirogov
    Moscow, Russian Federation
    Recruiting
  • Privolzhsky district medical center
    Nizhny Novgorod, Russian Federation
    Recruiting
  • State Novosibirsk Regional Clinical Hospital
    Novosibirsk, Russian Federation
    Recruiting
    • Vladimir Kohno, MD · Contactkair2007@mail.ru
    • Vladimir Kohno, MD · Principal investigator
  • Orenburg Regional Clinical Hospital
    Orenburg, Russian Federation
    Recruiting
  • "Republican hospital named after V. A. Baranov"
    Petrozavodsk, Russian Federation
    Recruiting
    • Arina Spasova, PhD · Contactarina22@mail.ru
    • Arina Spasova, PhD · Principal investigator
  • Rostov State Medical University
    Rostov-on-Don, Russian Federation
    Recruiting
    • Dmitry Martynov, PhD · Contactdvmartyn@mail.ru
    • Dmitry Martynov, PhD · Principal investigator
  • North-West State Medical University named after I.I.Mechnikov
    Saint Petersburg, Russian Federation
    Recruiting
    • Konstantin Lebedinski, MD · Contactmail@lebedinski.com
    • Konstantin Lebedinski, MD · Principal investigator
  • St. Petersburg state budgetary healthcare institution " City clinical Oncology dispensary"
    Saint Petersburg, Russian Federation
    Recruiting
    • Azam Khalikov, PhD · Contactjawlan2@gmail.com
    • Azam Khalikov, PhD · Principal investigator
  • "Samara Regional Clinical Oncology Dispensary"
    Samara, Russian Federation
    Recruiting
    • Vladimir Stadler, PhD · Contactev.stadler@mail.ru
    • Vladimir Stadler, PhD · Principal investigator
  • Clinical Hospital named after SR. Mirotvortseva (FGBOU VO "Saratov State Medical University. n.a. V.I.Razumovsky" Ministry of Health of the Russian Federation
    Saratov, Russian Federation
    Recruiting
    • Mikhail Prigorodov, MD · Contact
    • Mikhail Prigorodov, MD · Principal investigator
  • Stavropol regional clinical hospital
    Stavropol', Russian Federation
    Recruiting
  • Regional Clinical Hospital No. 1
    Tyumen, Russian Federation
    Not yet recruiting
    • Natalya Schen · Contact
  • Regional clinical hospital №2
    Vladivostok, Russian Federation
    Recruiting
    • Pavel Dunts, PhD · Contactdpv@bk.ru
    • Pavel Dunts, PhD · Principal investigator
  • Emergency hospital
    Volgograd, Russian Federation
    Recruiting
    • Alexandr Popov, MD · Contactairvma@yandex.ru
    • Alexandr Popov, MD · Principal investigator
  • Volgograd regional clinical hospital
    Volgograd, Russian Federation
    Recruiting
    • Alexandr Popov, MD · Contactairvma@yandex.ru
    • Alexandr Popov, MD · Principal investigator
  • Yakut Republican Oncological Dispensary
    Yakutsk, Russian Federation
    Recruiting
    • Afanasiy Matveev, MD · Contact
08

References and documents

Publications

  • Global patient outcomes after elective surgery: prospective cohort study in 27 low-, middle- and high-income countries. Br J Anaesth. 2017 Sep 1;119(3):553. doi: 10.1093/bja/aew472. No abstract available. PubMed 28498884 ↗
  • Weiser TG, Haynes AB, Molina G, Lipsitz SR, Esquivel MM, Uribe-Leitz T, Fu R, Azad T, Chao TE, Berry WR, Gawande AA. Size and distribution of the global volume of surgery in 2012. Bull World Health Organ. 2016 Mar 1;94(3):201-209F. doi: 10.2471/BLT.15.159293. PubMed 26966331 ↗
  • Gawande AA, Thomas EJ, Zinner MJ, Brennan TA. The incidence and nature of surgical adverse events in Colorado and Utah in 1992. Surgery. 1999 Jul;126(1):66-75. doi: 10.1067/msy.1999.98664. PubMed 10418594 ↗
  • Kable AK, Gibberd RW, Spigelman AD. Adverse events in surgical patients in Australia. Int J Qual Health Care. 2002 Aug;14(4):269-76. doi: 10.1093/intqhc/14.4.269. PubMed 12201185 ↗
  • Malik OS, Brovman EY, Urman RD. The Use of Regional or Local Anesthesia for Carotid Endarterectomies May Reduce Blood Loss and Pulmonary Complications. J Cardiothorac Vasc Anesth. 2019 Apr;33(4):935-942. doi: 10.1053/j.jvca.2018.08.195. Epub 2018 Aug 23. PubMed 30243870 ↗
  • Young J, Badgery-Parker T, Dobbins T, Jorgensen M, Gibbs P, Faragher I, Jones I, Currow D. Comparison of ECOG/WHO performance status and ASA score as a measure of functional status. J Pain Symptom Manage. 2015 Feb;49(2):258-64. doi: 10.1016/j.jpainsymman.2014.06.006. Epub 2014 Jul 1. PubMed 24996034 ↗
  • Whiteley MS, Prytherch DR, Higgins B, Weaver PC, Prout WG. An evaluation of the POSSUM surgical scoring system. Br J Surg. 1996 Jun;83(6):812-5. doi: 10.1002/bjs.1800830628. PubMed 8696749 ↗
  • Watt J, Tricco AC, Talbot-Hamon C, Pham B, Rios P, Grudniewicz A, Wong C, Sinclair D, Straus SE. Identifying older adults at risk of harm following elective surgery: a systematic review and meta-analysis. BMC Med. 2018 Jan 12;16(1):2. doi: 10.1186/s12916-017-0986-2. PubMed 29325567 ↗
  • Monk TG, Saini V, Weldon BC, Sigl JC. Anesthetic management and one-year mortality after noncardiac surgery. Anesth Analg. 2005 Jan;100(1):4-10. doi: 10.1213/01.ANE.0000147519.82841.5E. PubMed 15616043 ↗
  • van Diepen S, Bakal JA, McAlister FA, Ezekowitz JA. Mortality and readmission of patients with heart failure, atrial fibrillation, or coronary artery disease undergoing noncardiac surgery: an analysis of 38 047 patients. Circulation. 2011 Jul 19;124(3):289-96. doi: 10.1161/CIRCULATIONAHA.110.011130. Epub 2011 Jun 27. PubMed 21709059 ↗
  • Hachenberg T, Schneemilch C. Anesthesia in neurologic and psychiatric diseases: is there a 'best anesthesia' for certain diseases? Curr Opin Anaesthesiol. 2014 Aug;27(4):394-402. doi: 10.1097/ACO.0000000000000098. PubMed 24979067 ↗
  • Pearse RM, Moreno RP, Bauer P, Pelosi P, Metnitz P, Spies C, Vallet B, Vincent JL, Hoeft A, Rhodes A; European Surgical Outcomes Study (EuSOS) group for the Trials groups of the European Society of Intensive Care Medicine and the European Society of Anaesthesiology. Mortality after surgery in Europe: a 7 day cohort study. Lancet. 2012 Sep 22;380(9847):1059-65. doi: 10.1016/S0140-6736(12)61148-9. PubMed 22998715 ↗

Individual participant data

Plan to share: No

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Started Jul 2019 (actual). Primary completion is estimated for Dec 2025, 77 months after the start.

Of 132 non-industry observational studies under Coronary Disease, half reached primary completion within 59 months of starting (the median), counting those still running; a quarter within 24 and three quarters within 192. This study's planned 77 months is above that.

Counting every sponsor, half of 154 studies reached it within 47 months; a quarter within 21 and three quarters within 123.

How these figures are worked out, and which studies are left out of them.

Registered
May 9, 2019
First posted
May 10, 2019
StartActual
Jul 1, 2019
Primary completionEst.
Dec 30, 2025
CompletionEst.
Feb 28, 2026
Last update
Apr 4, 2025
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Apr 4, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT03945968
Lead sponsor
Russian Federation of Anesthesiologists and Reanimatologists
Collaborators
Kuban State Medical University
Responsible party
Igor Zabolotskikh (Head of guidelines and clinical stгdies commettee, Russian Federation of Anesthesiologists and Reanimatologists) — Principal investigator
First posted
May 10, 2019
Start date
Jul 1, 2019
Primary completion
Dec 30, 2025 (estimated)
Completion
Feb 28, 2026 (estimated)
Last update
Apr 4, 2025

Study contacts

Nikita Trembach, PhD
Contact
nikitkax@mail.ru
+79528589299
Igor Zabolotskikh, MD
Contact
pobeda_zib@mail.ru
Igor Zabolotskikh, MD
principal investigator · Russian Federation of Anesthesiologists and Reanimatologists

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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