Availability of Venous Conduits in Patients With Varicose Veins for Arterial Bypass Surgery

March 22, 2024 updated by: Pirogov Russian National Research Medical University
Patients with PAD having superficial femoral artery (SFA) occlusion were consecutively enrolled. Demographic data and medical history were taken. Physical examination and duplex ultrasound were performed.

Study Overview

Status

Recruiting

Conditions

Detailed Description

Patients with PAD having superficial femoral artery (SFA) occlusion were consecutively enrolled. Demographic data and medical history were taken. Physical examination and duplex ultrasound were performed. The investigators registered presence of varicose veins, type of previous invasive procedure and availability of saphenous trunks as possible grafts

Study Type

Observational

Enrollment (Estimated)

80

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • Russian Federation
    • Pirogov Russian National Research Medical University
      • Moscow, Pirogov Russian National Research Medical University, Russian Federation, 109044
        • Recruiting
        • Veronika Golovina
        • Contact:

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Sampling Method

Probability Sample

Study Population

Patients with PAD having superficial femoral artery (SFA) occlusion.

Description

Inclusion Criteria:

  • Older than 18 Years

Exclusion Criteria:

  • Those unwilling to sign an informed consent were also included.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
availability of saphenous trunks as possible grafts
Time Frame: at the moment of inclusion
availability of saphenous trunks as possible grafts (Yes|No)
at the moment of inclusion

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
presence of varicose veins
Time Frame: at the moment of inclusion
presence of varicose veins (Yes|No)
at the moment of inclusion
type of previous invasive procedure
Time Frame: at the moment of inclusion
Phlebectomy\ radiofrequency ablation\ endovenous laser ablation (Yes|No)
at the moment of inclusion

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Pirogov Russian National Research Medical University

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

December 1, 2023

Primary Completion (Estimated)

May 31, 2024

Study Completion (Estimated)

May 31, 2024

Study Registration Dates

First Submitted

March 15, 2024

First Submitted That Met QC Criteria

March 22, 2024

First Posted (Actual)

March 27, 2024

Study Record Updates

Last Update Posted (Actual)

March 27, 2024

Last Update Submitted That Met QC Criteria

March 22, 2024

Last Verified

December 1, 2023

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

  • 235

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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