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A Comparative Study of the Effectiveness of Radial Artery and No-touch Vein in Coronary Artery Bypass Grafting in Women

Status: Recruiting
Location: See location...
Intervention Type: Procedure
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

This study examines the outcomes of coronary artery bypass grafting (CABG) in women at 1 year after surgery. A randomized controlled trial is planned, including a comparative analysis of two observed groups depending on the chosen conduit for revascularization of the circumflex artery. The main group is supposed to include 55 patients undergoing CABG with the use of the radial artery, while the control group will include 55 patients undergoing CABG with the use of the great saphenous vein prepared using the no-touch technique.

Eligibility
Participation Requirements
Sex: Female
Minimum Age: 18
Healthy Volunteers: f
View:

• Three-vessel disease involving the target circumflex artery with stenosis ≥70% and a diameter ≥1.5 mm

• Females aged 18 years and older

• Signed informed consent

• Clinical indications for coronary revascularization (refractory angina/transient myocardial ischemia according to noninvasive tests)

Locations
Other Locations
Russian Federation
Cardiology Research Institute, Tomsk National Research Medical Center, Russian Academy of Sciences, Tomsk, Russia
RECRUITING
Tomsk
Contact Information
Primary
Vasily V. Zatolokin, PhD
zatolokin@cardio-tomsk.ru
+79138490545
Backup
Danil V. Timofeev
3120v@mail.ru
+79059937497
Time Frame
Start Date: 2026-04-06
Estimated Completion Date: 2029-04
Participants
Target number of participants: 110
Treatments
Active_comparator: Radial artery
Radial artery as a conduit for the circumflex artery territory in 55 patients undergoing coronary artery bypass grafting
Active_comparator: No-touch great saphenous vein
No-touch great saphenous vein graft for revascularization of the circumflex artery territory in 55 patients during coronary artery bypass grafting
Sponsors
Leads: Tomsk Cardiology Research Institute

This content was sourced from clinicaltrials.gov

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