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Recruiting NCT03881345

Ongoing Registry of Treatment of Venous Thromboembolism

— Observational Deep Vein Thrombosis Thromboses, Venous Thrombosis Embolism Postthrombotic Syndrome

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Anticoagulants, Open surgery, Thrombolysis, Venous stenting.
Who it may be relevant to
Registry conditions: Deep Vein Thrombosis, Thromboses, Venous, Thrombosis Embolism, Postthrombotic Syndrome. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Russia
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Official title

Russian Registry of Treatment of Venous Thromboembolism

Overview

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

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

Interventions

  • Drug Anticoagulants
    anticoagulation according to the main diagnosis
  • Procedure Open surgery
    removal of blood clots with open surgery
  • Procedure Thrombolysis
    removal of blood clots with thrombolysis
  • Procedure Venous stenting
    elimination of vein obstruction by stenting

Primary outcome measures

  • Veins patency [Time frame: Baseline, 3 and 12 months post-intervention]
Secondary outcome measures (3)
  • Postthrombotic syndrome [Time frame: Baseline, 3 and 12 months post-intervention]
  • QoL SF-36 [Time frame: Baseline, 3 and 12 months post-intervention]
  • QoL AVVQ [Time frame: Baseline, 3 and 12 months post-intervention]

Eligibility criteria

Inclusion criteria

  • case of venous thrombosis of a limb or pulmonary embolus

Exclusion criteria

  • no exclusion criteria

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Other

Study locations

Russia · 1 center
  • Pirogov Russian National Research Medical University — Moscow

Identifiers

NCT: NCT03881345 · A002

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗