Complications and Antiplatelet and Anticoagulant Therapy in Vascular Surgery.
Determination the Safety of Disaggregant and Anticoagulant Therapy in the Development of Complications in Noncardiac Vascular Surgery.
1 other identifier
observational
500
1 country
1
Brief Summary
The goal of this retrospective clinical trial is to find out association antiplatelet and anticoagulant therapy with perioperative complications in non-cardiac vascular surgery in patients . The main questions it aims to answer are: Does the use of antiplatelet agents and anticoagulants affect the development of complications in the perioperative period during operations on the main arteries? Does discontinuing antiplatelet and anticoagulant medications affect the development of perioperative complications in major artery surgeries?? Researchers will compare with patients who didn't use antiplatelets and anticoagulant drugs to see ift he incidence of complications comparable? This is a retrospective study based on the analysis of medical records (case histories).
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started May 2025
Shorter than P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
May 1, 2025
CompletedFirst Submitted
Initial submission to the registry
January 14, 2026
CompletedFirst Posted
Study publicly available on registry
January 22, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
February 12, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
February 28, 2026
CompletedJanuary 22, 2026
January 1, 2026
10 months
January 14, 2026
January 14, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Bleeding
Case of bleeding or haematoma development
First 24 hours after operation
Secondary Outcomes (1)
Trombosis
First 24 hours after operation
Study Arms (3)
Control
Patients who did not take antiplatelet agents and anticoagulants
Antiplatelet and anticoagulants
Patients who use antiplatelet agents and anticoagulants until the operation day
Discontinuation of antiplatelet and anticoagulants
Patients who discontinuate antiplatelet agents and anticoagulants until the operation day
Interventions
Patients who take aspirin and clopidogrel until the operation day
Patients who take aspirin and ticagrelor until the operation day
Patients who take aspirin and apixaban until the operation day
Patients who take aspirin and rivaroxaban until the operation day
Patients who take clopidogrel and apixaban until the operation day
Patients who take clopidogrel and rivaroxaban until the operation day
Eligibility Criteria
Patients with surgical treatment of atherosclerotic lesions of the main arteries.
You may qualify if:
- Patients who received surgical treatment on the main arteries.
You may not qualify if:
- Patients who received surgical treatment on the main veins.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
NRCS Petrovsky
Moscow, 119991, Russia
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- RETROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
January 14, 2026
First Posted
January 22, 2026
Study Start
May 1, 2025
Primary Completion
February 12, 2026
Study Completion
February 28, 2026
Last Updated
January 22, 2026
Record last verified: 2026-01
Data Sharing
- IPD Sharing
- Will share