ClinicalTrials.gg
RecruitingNCT03881345RRT VTEUpdated May 8, 2025

Ongoing Registry of Treatment of Venous Thromboembolism

An observational study in Deep Vein Thrombosis, Thromboses, Venous and Thrombosis Embolism, sponsored by Medalp Private Surgery Clinic. Recruiting at 1 site in Russian Federation. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2025-05-08.

Primary conditionPostthrombotic SyndromeRegistry: Venous ThrombosisReclassifiedWhy we changed it
Registry
Venous Thrombosis — the first condition term the registry derived for this study.
ClinicalTrials.gg
Postthrombotic Syndrome
Why
  1. The study's listed conditions name Postthrombotic Syndrome, a narrower term within Venous Thrombosis.
Confidence
High: the new condition is named in the study's own listed conditions. Of 351 hand-checked studies reclassified this way, 68% were exactly right and 84% in the right disease family; the registry's first term was right for 5% (measured 2026-10-21). How we classify →
Wrong?
Tell us the study's main condition →

Sponsored by Medalp Private Surgery Clinic · Observational

From the registry’s dates

  • Started Apr 2019; still recruiting 7 years 7 months later.
Study type
Observational
Model
Other
Time perspective
Prospective
Enrollment
5,000
Ages
18 Years and older
Sex
All
01

Study summary

Ongoing registration of patients with venous thromboembolism treated by means of antithrombotic therapy, thrombolisys, open surgery, endovenous desobstruction and stenting.

Read the detailed description

Data of patients with VTE treated in different Russian medical centers are entered in a prospective digital database, and continuously updated.

There is planned to conduct prospective randomized, cohort and observational studies on the site of register

02

Conditions studied

  • Deep Vein Thrombosis
  • Thromboses, Venous
  • Thrombosis Embolism
  • Postthrombotic Syndrome
  • Pulmonary Embolism
03

In context

Postthrombotic Syndrome Reclassified

73 studies on the registry are indexed under Postthrombotic Syndrome; 21 are open to participants now.

This study's planned enrollment of 5,000 is above the median of 288 across 23 observational studies indexed under Postthrombotic Syndrome.

Browse Postthrombotic Syndrome studies →

Lead sponsor

Medalp Private Surgery Clinic is the lead sponsor of 2 studies on the registry; 2 are open to participants now.

Compared within Postthrombotic Syndrome, this study's primary condition as ClinicalTrials.gg classifies it; the registry's first condition term is Venous Thrombosis. The counts are of registry records indexed under each term, refreshed daily. How we classify →

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Patients undergoing any kind of treatment for venous thromboembolism

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

  • case of venous thrombosis of a limb or pulmonary embolus

Exclusion criteria

Exclusion Criteria:

  • no exclusion criteria
05

Study design

Observational model
Other
Time perspective
Prospective
Enrollment
5,000 participants (estimated)
Target follow-up
12 Months
Patient registry
Yes

Interventions

  • DrugAnticoagulants

    anticoagulation according to the main diagnosis

  • ProcedureOpen surgery

    removal of blood clots with open surgery

  • ProcedureThrombolysis

    removal of blood clots with thrombolysis

  • ProcedureVenous stenting

    elimination of vein obstruction by stenting

06

What researchers measure

Primary outcomes

  1. Veins patency

    Change in patency target veins assessed by duplex ultrasonography in different follow up periods due to different treatment methods

    Time frame: Baseline, 3 and 12 months post-intervention

Secondary outcomes

  1. Postthrombotic syndrome

    the presence and severity of postthrombotic syndrome on the Villalta scale

    Time frame: Baseline, 3 and 12 months post-intervention

  2. QoL SF-36

    Change in Quality of Life (QoL), assessed by "Short form 36" health survey (SF-36). Total scale range: from 0 to 800. SF-36 consists of 8 subscales. Each subscale range: 0 - 100. Subscales are combined using a special algorithm described in the instructions for the SF-36. For total scale the higher value represent the worse QoL.

    Time frame: Baseline, 3 and 12 months post-intervention

  3. QoL AVVQ

    Change in Quality of Life (QoL), assessed by "Aberdeen Varicose Vein Questionnaire" (AVVQ). The AVVQ is a disease-specific QoL questionnaire aimed at venous disease. Total scale range: from 0 to 100, where the higher score represent worse QoL.

    Time frame: Baseline, 3 and 12 months post-intervention

07

Study locations

1 of 1 sites recruiting
  • Pirogov Russian National Research Medical University
    Moscow, 190000, Russian Federation
    Recruiting
    • Yury Stoyko, MD, PhD · Contact
08

References and documents

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Started Apr 2019 (actual). Primary completion is estimated for Mar 2036, 203 months after the start.

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

Registered
Mar 17, 2019
First posted
Mar 19, 2019
StartActual
Apr 1, 2019
Primary completionEst.
Mar 1, 2036
CompletionEst.
Mar 1, 2036
Last update
May 8, 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 May 8, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT03881345
Lead sponsor
Medalp Private Surgery Clinic
Collaborators
State Budgetary Healthcare Institution, National Medical Surgical Center N.A. N.I. Pirogov, Ministry of Health of Russia
Responsible party
Evgeny Ilyukhin (Principal Investigator, Medalp Private Surgery Clinic) — Principal investigator
First posted
Mar 19, 2019
Start date
Apr 1, 2019
Primary completion
Mar 1, 2036 (estimated)
Completion
Mar 1, 2036 (estimated)
Last update
May 8, 2025

Study contacts

Evgeny Ilyukhin
Contact
evgeny@ilyukhin.info
+79218451722

Oversight

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

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