Randomised comparison of radial versus femoral access for coronary angioplasty in the ReoPro era
| ISRCTN | ISRCTN49416601 |
|---|---|
| DOI | https://doi.org/10.1186/ISRCTN49416601 |
| Secondary identifying numbers | N0205116657 |
- Submission date
- 12/09/2003
- Registration date
- 12/09/2003
- Last edited
- 18/10/2016
- Recruitment status
- No longer recruiting
- Overall study status
- Completed
- Condition category
- Surgery
Prospectively registered
Protocol
Statistical analysis plan
Results
Individual participant data
Record updated in last year
Plain English summary of protocol
Not provided at time of registration
Contact information
Dr Richard Schilling
Scientific
Scientific
Department of Cardiology
Dominion House
Bartholomew's Close
St Bartholomew's Hospital
London
EC1A 7BE
United Kingdom
| r.schilling@qmul.ac.uk |
Study information
| Study design | Randomised controlled trial |
|---|---|
| Primary study design | Interventional |
| Secondary study design | Randomised controlled trial |
| Study setting(s) | Hospital |
| Study type | Treatment |
| Participant information sheet | Not available in web format, please use contact details to request a participant information sheet |
| Scientific title | Randomised comparison of radial versus femoral access for coronary angioplasty in the ReoPro era |
| Study acronym | DA7RAD study |
| Study objectives | When using ReoPro during percutaneous coronary intervention (PCI): 1. Is the vascular complication rate less than when radial access rather than femoral access? 2. Is mobilisation early safe, is patient satisfaction improved? |
| Ethics approval(s) | Not provided at time of registration |
| Health condition(s) or problem(s) studied | Percutaneous coronary angioplasty |
| Intervention | Randomised prospective clinical trial: radial versus femoral access for coronary angioplasty. |
| Intervention type | Procedure/Surgery |
| Primary outcome measure | 1. Access site complications 2. Time to mobilisation 3. Patient satisfaction |
| Secondary outcome measures | Not provided at time of registration |
| Overall study start date | 01/11/2002 |
| Completion date | 01/06/2004 |
Eligibility
| Participant type(s) | Patient |
|---|---|
| Age group | Not Specified |
| Sex | Not Specified |
| Target number of participants | Not provided at time of registration |
| Key inclusion criteria | Patients undergoing percutaneous coronary angioplasty at Barts and The London NHS Trust |
| Key exclusion criteria | Not provided at time of registration |
| Date of first enrolment | 01/11/2002 |
| Date of final enrolment | 01/06/2004 |
Locations
Countries of recruitment
- England
- United Kingdom
Study participating centre
St Bartholomew's Hospital
London
EC1A 7BE
United Kingdom
EC1A 7BE
United Kingdom
Sponsor information
Department of Health (UK)
Government
Government
Richmond House
79 Whitehall
London
SW1A 2NL
United Kingdom
| Website | http://www.doh.gov.uk |
|---|
Funders
Funder type
Government
Barts and The London NHS Trust (UK)
No information available
Results and Publications
| Intention to publish date | |
|---|---|
| Individual participant data (IPD) Intention to share | No |
| IPD sharing plan summary | Not provided at time of registration |
| Publication and dissemination plan | Not provided at time of registration |
| IPD sharing plan |
Editorial Notes
18/10/2016: No publications found, verifying study status with principal investigator.
