Clinical Trial

Time to Ambulation After ProGlide Closure

Study acronym: OPTIMA
Recruiting
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Record status
This record was last updated January 23, 2026 (before its estimated March 30, 2026 completion). Its status may not reflect the trial's current state.
Summary
Transradial access has become the standard for coronary procedures due to fewer vascular complications and shorter bed rest, yet transfemoral access remains essential for complex peripheral interventions requiring larger sheaths and stronger support. Vascular closure devices (VCDs), particularly suture-mediated devices such as ProGlide, have improved femoral access by reducing hemostasis time, ambulation delay, and patient discomfort. Although early ambulation after ProGlide closure has been reported, current practice varies widely, and the relationship between ambulation timing and vascular complications remains unclear. This trial aims to evaluate the effect of different ambulation times after ProGlide closure in transfemoral peripheral angiography or intervention, with the goal of identifying the optimal time to ambulation that balances safety and efficiency.
Protocol Amendment History 1 amendment
This ClinicalTrials.gov record has been amended once since 2025-09-16.
Status change: Not Yet Recruiting → Recruiting 2026-01-21
Trial Details
NCT Number NCT07179536
Lead Sponsor Chinese Academy of Medical Sciences, Fuwai Hospital
Conditions Femoral Access Site Closure, Ambulation, Vascular Access Complication, Vascular Access Site Management
Enrollment 300 participants
Start Date 2025-10-01
Primary Completion 2026-03-30 (estimated)
Study Completion 2026-03-30 (estimated)
Updated on ClinicalTrials.gov 2026-01-23