NCT06688747Not yet recruiting
The Primary Endpoint is to Compare the Incidence of Forearm RAO Between Distal and Traditional Radial Access Assessed by Vascular Ultrasound At Discharge
Distal Versus Traditional Radial Access for Coronary Angiography and Intervention
Source: ClinicalTrials.gov · Last updated 14 Nov 2024 · Not updated for over 12 months - ask the site whether it is still open
Brief summary (registry, in English)
The primary endpoint is to compare the incidence of forearm RAO between distal and traditional radial access for coronary angiography and intervention
- Status (registry)
- Not yet recruiting
- Study type
- Observational
- Enrollment
- 230 (estimated)
- First submitted
- 11 Nov 2024
- Start date
- 1 Dec 2024
- Primary completion date
- 1 Dec 2025
- Lead sponsor
- Assiut University
- NCT number
- NCT06688747
What you commit to
- Study type: Observational
- Planned participants: 230
- From 1 Dec 2024 to the primary completion date, 1 Dec 2025
- No sites listed in no country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Other
- Chronic hemodialysis
- Treatment of a coronary chronic total occlusion (CTO) lesion
- Patients who underwent CA or PCI with radial access before
Who the study is looking for
- Aged ≥18 y
- Signed informed consent form
- Indication to diagnostic coronary angiography or PCI
- Patient's suitability for both DRA and conventional TRA using 6 Fr Sheath
Sex: All · Does not accept healthy volunteers
This page is information, not medical advice. Discuss any trial with your doctor.