Distal Versus Conventional Transradial Artery Access for Coronary Catheterization in Patients With ST-elevation Myocardial Infraction (STEMI): The DR-STEMI Trial

Status: Recruiting
Location: See all (3) locations...
Intervention Type: Procedure
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

Recently, a novel distal transradial, through anatomical snuffbox, approach has been proposed for undertaking percutaneous coronary angiography and interventions. The existing literature has evaluated distal transradial access (dTRA) as a feasible and safe approach, with faster hemostasis, lower rates of periprocedural complications and reduced incidence of radial artery occlusion (RAO). Aim of the present study is to compare dTRA versus conventional TRA access in patients with STEMI undergoing coronary angiography and interventions regarding peri- and post-procedural characteristics.

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

• Age \> 18 years old

• Indication: ST-Elevation Myocardial Infraction

Locations
Other Locations
Belgium
Department of Cardiology, Centre Hospitalier Universitaire de Charleroi
RECRUITING
Charleroi
Greece
University Hospital of Patras
RECRUITING
Pátrai
Switzerland
Department of Cardiology, Geneva University Hospitals, Geneva, Switzerland.
RECRUITING
Geneva
Contact Information
Primary
Grigorios Tsigkas, MD, PhD
gregtsig@hotmail.com
+306974466662
Backup
Adel Aminian, MD, PhD
adaminian@hotmail.com
Time Frame
Start Date: 2024-05-23
Estimated Completion Date: 2025-12-01
Participants
Target number of participants: 554
Treatments
Experimental: Distal transradial artery access
Vascular access after cannulation of distal transradial artery through anatomical snuffbox for coronary angiography and interventions
Active_comparator: Conventional transradial artery access
Vascular access after puncturing on the conventional transradial artery for performing coronary angiography and interventions
Sponsors
Leads: University Hospital of Patras

This content was sourced from clinicaltrials.gov