Ongoing Registry of Treatment of Venous Thromboembolism
RRT VTE
Russian Registry of Treatment of Venous Thromboembolism
1 other identifier
observational
5,000
1 country
1
Brief Summary
Ongoing registration of patients with venous thromboembolism treated by means of antithrombotic therapy, thrombolisys, open surgery, endovenous desobstruction and stenting.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Apr 2019
Longer than P75 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
March 17, 2019
CompletedFirst Posted
Study publicly available on registry
March 19, 2019
CompletedStudy Start
First participant enrolled
April 1, 2019
CompletedPrimary Completion
Last participant's last visit for primary outcome
March 1, 2036
ExpectedStudy Completion
Last participant's last visit for all outcomes
March 1, 2036
May 8, 2025
May 1, 2025
16.9 years
March 17, 2019
May 5, 2025
Conditions
Outcome Measures
Primary Outcomes (1)
Veins patency
Change in patency target veins assessed by duplex ultrasonography in different follow up periods due to different treatment methods
Baseline, 3 and 12 months post-intervention
Secondary Outcomes (3)
Postthrombotic syndrome
Baseline, 3 and 12 months post-intervention
QoL SF-36
Baseline, 3 and 12 months post-intervention
QoL AVVQ
Baseline, 3 and 12 months post-intervention
Interventions
anticoagulation according to the main diagnosis
removal of blood clots with open surgery
removal of blood clots with thrombolysis
elimination of vein obstruction by stenting
Eligibility Criteria
Patients undergoing any kind of treatment for venous thromboembolism
You may qualify if:
- case of venous thrombosis of a limb or pulmonary embolus
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Pirogov Russian National Research Medical University
Moscow, Moscow, 190000, Russia
Related Links
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- OTHER
- Time Perspective
- PROSPECTIVE
- Target Duration
- 12 Months
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Principal Investigator
Study Record Dates
First Submitted
March 17, 2019
First Posted
March 19, 2019
Study Start
April 1, 2019
Primary Completion (Estimated)
March 1, 2036
Study Completion (Estimated)
March 1, 2036
Last Updated
May 8, 2025
Record last verified: 2025-05
Data Sharing
- IPD Sharing
- Will not share