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CompletedNCT05354648Updated Jun 9, 2026

Effects of Hypoxic-hyperoxic Preconditioning in Cardio-surgical Patients

An interventional study of Hypoxic-hyperoxic preconditioning and Placebo in Myocardial Reperfusion Injury, Hypoxia and Hyperoxia, sponsored by Alexander Averyanov. Completed. Open to participants aged 18 Years to 75 Years. Per ClinicalTrials.gov, last updated 2026-06-09.

Sponsored by Alexander Averyanov · Not applicable, Interventional, and Prevention

From the registry’s dates

  • Registered 6 years 10 months after the study started (first participant enrolled Jun 2015, registered Apr 2022).
Phase
Not applicable
Study type
Interventional
Enrollment
120
Allocation
Randomized
Ages
18 Years to 75 Years
Sex
All
01

Study summary

Coronary artery bypass grafting (CABG) with cardiopulmonary bypass is a common surgical therapy for patients suffering from coronary artery diseases. The heart is subjected to a long period of ischemia due to the occlusion of the aorta. The heavy burden of myocardial ischemia-reperfusion injury (IRI) thus induces cardiomyocyte death, which can paradoxically reduce the beneficial effect of CABG. Preconditioning by moderate hypoxia or hyperoxia serves as an effective drug-free method to increase the organism's resistance to negative effects, including IRI.

Read the detailed description

It has been firmly established that the diminished oxygen delivery to the tissues in response to hypoxia is countered by a combination of the increased regional blood flow and the enhanced functional capillary density in the microcirculation. In experimental studies, exposure to hyperoxia for a limited time before ischemia induces a low-grade systemic oxidative stress evokes a preconditioning-like effect on the myocardium and reduces the infarction area by 20%, and the number of arrhythmias after ischemia-reperfusion. One hundred twenty patients were randomly assigned into two equal groups: hypoxic-hyperoxic preconditioning before the surgery (HHP group) and the control group (without preconditioning). Safety control of the preconditioning procedure included ECG monitoring, invasive blood pressure, cardiac output, pulse oximetry, capnography, cerebral oximetry, measurement of anaerobic threshold; acid-base status and metabolic state of arterial and venous blood were assessed once every 10 min during the preconditioning procedure; oxygen balance parameters were calculated. Seventy-two hours before the surgery, an anaerobic threshold was determined to establish a safe oxygen concentration in the respiratory gas mixture during the hypoxic preconditioning phase from 10 to 14%, followed by 75-80% oxygen concentration during the hyperoxic phase.

The hypoxic-hyperoxic preconditioning with individual parameters selection based on the anaerobic threshold in patients with coronary artery diseases before the main stage of cardiac surgery with a cardiopulmonary bypass should reduce the duration of mechanical ventilation, catecholamine support, and frequency of perioperative complications.

02

Conditions studied

  • Myocardial Reperfusion Injury
  • Hypoxia
  • Hyperoxia
  • Coronary Artery Disease

Keywords

  • myocardial protection
  • preconditioning
  • hypoxia
  • hyperoxia
  • ischemia-reperfusion injury
  • cardiopulmonary bypass
  • oxygen transport
03

In context

Myocardial Reperfusion Injury

57 studies on the registry are indexed under Myocardial Reperfusion Injury; 6 are open to participants now.

This study's enrollment of 120 is above the median of 81 across 46 interventional studies indexed under Myocardial Reperfusion Injury.

Browse Myocardial Reperfusion Injury studies →

Lead sponsor

Alexander Averyanov is the lead sponsor of 2 studies on the registry; none are open to participants now.

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

04

Who can participate

Ages eligible
18 Years to 75 Years
Sexes eligible
All
Accepts healthy volunteers
No

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

  • the need for coronary artery bypass grafting (CABG)

Exclusion criteria

Exclusion Criteria:

  • age over 75 years
  • emergency surgery
  • diabetes mellitus
  • exacerbation of a chronic disease 1 week before surgery
  • any oncological disease at the time of the examination
05

Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Participant, Care provider)
Enrollment
120 participants (actual)

Study arms

  • Active comparator
    Hypoxic-hyperoxic preconditioning (HHP)

    HHP was carried out as follows: breathing with a hypoxic gas mixture for 10 min with the development of hypoxemia, then breathing with a hyperoxic gas mixture for 30 minutes, and at the last stage, a period of breathing with atmospheric air until the cardio-pulmonary bypass is connected. The anaerobic threshold was determined 72 hours before surgery to establish a safe oxygen concentration in the respiratory gas mixture during the hypoxic phase of preconditioning.

    Procedure: Hypoxic-hyperoxic preconditioning

  • Placebo comparator
    Control

    The anaerobic threshold was determined, however, patients in the control group were not preconditioned. Mechanical ventilation was carried out with individual settings maintaining the target values of PaO2 and PaCO2 (80 - 120 mm Hg and 35 - 45 mm Hg, respectively), until the cardio-pulmonary bypass was connected.

    Procedure: Placebo

Interventions

  • ProcedureHypoxic-hyperoxic preconditioning

    Patients were intubated and mechanically ventilated with the target values of PaO2 and PaCO2 (80 - 120 mm Hg and 35 - 45 mm Hg, respectively) under the inhalation anesthesia. HHP was carried out as follows: breathing with a hypoxic gas mixture for 10 min with the development of hypoxemia, then breathing with a hyperoxic gas mixture for 30 minutes, then a period of breathing with atmospheric air (normoxia and normocapnia) until the cardio-pulmonary bypass is connected.

    Also known as: HHP

  • ProcedurePlacebo

    Patients were intubated and mechanically ventilated with the target values of PaO2 and PaCO2 (80 - 120 mm Hg and 35 - 45 mm Hg, respectively) under the inhalation anesthesia until the cardio-pulmonary bypass is connected.

06

What researchers measure

Primary outcomes

  1. Number of Participants with complications

    Any type of complications in postoperative period

    Time frame: 60 days

  2. Mechanical ventilation

    Mechanical ventilation time

    Time frame: 60 days

  3. Rate of spontaneous sinus rhythm recovery

    Spontaneous sinus rhythm recovery after surgery

    Time frame: 14 days

Secondary outcomes

  1. Catecholamine support

    Catecholamine support time

    Time frame: 60 days

  2. Troponin T

    Troponin T concentration

    Time frame: 12 hours

  3. Endothelin-1

    Endothelin-1 concentrations

    Time frame: 1 day before surgery

  4. Endothelin-1 dynamics 1

    Endothelin-1 concentrations

    Time frame: at the end of surgery

  5. Endothelin-1 dynamics 2

    Endothelin-1 concentrations

    Time frame: 24 hours after surgery

  6. NOx total

    NOx total concentrations

    Time frame: 1 day before surgery

  7. NOx total dynamics 1

    NOx total concentrations

    Time frame: at the end of surgery

  8. NOx total dynamics 2

    NOx total concentrations

    Time frame: 24 hours after surgery

  9. Asymmetric dimethylarginine (ADMA)

    ADMA concentrations

    Time frame: 1 day before surgery

  10. ADMA dymanics 1

    ADMA concentrations

    Time frame: at the end of surgery

  11. ADMA dymanics 2

    ADMA concentrations

    Time frame: 24 hours after surgery

07

Study locations

No study locations are listed for this record.

08

References and documents

Publications

  • Mandel IA, Podoksenov YK, Suhodolo IV, An DA, Mikheev SL, Podoksenov AY, Svirko YS, Gusakova AM, Shipulin VM, Yavorovskiy AG. Influence of Hypoxic and Hyperoxic Preconditioning on Endothelial Function in a Model of Myocardial Ischemia-Reperfusion Injury with Cardiopulmonary Bypass (Experimental Study). Int J Mol Sci. 2020 Jul 27;21(15):5336. doi: 10.3390/ijms21155336. PubMed 32727110 ↗
09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 9, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05354648
Lead sponsor
Alexander Averyanov
Collaborators
Tomsk National Research Medical Center of the Russian Academy of Sciences, Siberian State Medical University, I.M. Sechenov First Moscow State Medical University
Responsible party
Alexander Averyanov (Professor, Federal Research Clinical Center of Federal Medical & Biological Agency, Russia) — Sponsor-investigator
First posted
Apr 29, 2022
Start date
Jun 1, 2015
Primary completion
Jan 15, 2016
Completion
Feb 22, 2016
Last update
Jun 9, 2026

Study contacts

Irina A Mandel, PhD
principal investigator · Federal Research Clinical Center FMBA Russia

Oversight

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

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This study is completed, as verified in Jun 2026. You cannot join it, but the record below documents what was studied.

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