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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06332833
Other study ID # 235
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date December 1, 2023
Est. completion date May 31, 2024

Study information

Verified date December 2023
Source Pirogov Russian National Research Medical University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

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.


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


Recruitment information / eligibility

Status Recruiting
Enrollment 80
Est. completion date May 31, 2024
Est. primary completion date May 31, 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Older than 18 Years Exclusion Criteria: - Those unwilling to sign an informed consent were also included.

Study Design


Locations

Country Name City State
Russian Federation Veronika Golovina Moscow Pirogov Russian National Research Medical University

Sponsors (1)

Lead Sponsor Collaborator
Pirogov Russian National Research Medical University

Country where clinical trial is conducted

Russian Federation, 

Outcome

Type Measure Description Time frame Safety issue
Primary availability of saphenous trunks as possible grafts availability of saphenous trunks as possible grafts (Yes|No) at the moment of inclusion
Secondary presence of varicose veins presence of varicose veins (Yes|No) at the moment of inclusion
Secondary type of previous invasive procedure Phlebectomy\ radiofrequency ablation\ endovenous laser ablation (Yes|No) at the moment of inclusion
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