Coronary Angiography Clinical Trial
— DIPRAOfficial title:
Distal vs. Proximal Radial Artery Access for Cardiac Catheterization and Intervention
Verified date | March 2020 |
Source | Baylor Research Institute |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
This single-center, prospective, randomized study will evaluate distal radial artery (dRA) vs. proximal radial artery access (pRA) in regards to hand function and radial artery occlusion.
Status | Completed |
Enrollment | 300 |
Est. completion date | December 31, 2022 |
Est. primary completion date | December 31, 2021 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: 1. Age = 18 years. 2. The distal and proximal radial artery must be palpable and non-occlusive flow must be confirmed by (Doppler) ultrasound. 3. Patient should be able to comply with the protocol. 4. Provide written informed consent before study participation Exclusion Criteria: 1. Obligatory femoral or forearm radial access 2. Previous ipsilateral forearm radial artery occlusion. 3. Patient on therapeutic oral anticoagulation. 4. Very large hand/wrist anatomy that will preclude using the available hemostatic radial bands. 5. Enrolment in another study that competes or interferes with this study. 6. Poor clinical condition like cardiogenic shock, which prohibits pre- and post-procedural function tests. 7. Subject with planned complex PCI or procedure necessitating multiple intervention. 8. Any other condition or co-morbidity which, in the opinion of the investigator or operator, may pose a significant hazard to the subject if he or she is enrolled in the study. 9. History of stroke with residual deficit that affects hand function. 10. Previous radial artery catheterization within 1 year. |
Country | Name | City | State |
---|---|---|---|
United States | Baylor Scott & White The Heart Hospital - Plano | Plano | Texas |
Lead Sponsor | Collaborator |
---|---|
Baylor Research Institute |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Quick Disabilities of the Arm Shoulder and Hand (DASH) Questionnaire Score (0-100) | Hand function questionnaire, Range: 0 (no disability) to 100 (most severe disability) | 1 year | |
Primary | Thumb and Forefinger Pinch Strength Test | Hand function: Thumb and forefinger pinch strength (kg) | 1 year | |
Primary | Hand Grip Strength Test | Hand grip strength test (kg) | 1 month | |
Secondary | Re-intervention Using the Radial Artery | Patients who required re-intervention using the radial artery up to 1 year following the initial intervention | 1 year | |
Secondary | Radial Artery Occlusion | Occurrence of distal radial artery occlusion and proximal radial artery occlusion for patients who had distal or proximal radial artery access | 1 year |
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