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

Department of Cardiology
Dominion House
Bartholomew's Close
St Bartholomew's Hospital
London
EC1A 7BE
United Kingdom

Email r.schilling@qmul.ac.uk

Study information

Study designRandomised controlled trial
Primary study designInterventional
Secondary study designRandomised controlled trial
Study setting(s)Hospital
Study typeTreatment
Participant information sheet Not available in web format, please use contact details to request a participant information sheet
Scientific titleRandomised comparison of radial versus femoral access for coronary angioplasty in the ReoPro era
Study acronymDA7RAD study
Study objectivesWhen 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) studiedPercutaneous coronary angioplasty
InterventionRandomised prospective clinical trial: radial versus femoral access for coronary angioplasty.
Intervention typeProcedure/Surgery
Primary outcome measure1. Access site complications
2. Time to mobilisation
3. Patient satisfaction
Secondary outcome measuresNot provided at time of registration
Overall study start date01/11/2002
Completion date01/06/2004

Eligibility

Participant type(s)Patient
Age groupNot Specified
SexNot Specified
Target number of participantsNot provided at time of registration
Key inclusion criteriaPatients undergoing percutaneous coronary angioplasty at Barts and The London NHS Trust
Key exclusion criteriaNot provided at time of registration
Date of first enrolment01/11/2002
Date of final enrolment01/06/2004

Locations

Countries of recruitment

  • England
  • United Kingdom

Study participating centre

St Bartholomew's Hospital
London
EC1A 7BE
United Kingdom

Sponsor information

Department of Health (UK)
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 shareNo
IPD sharing plan summaryNot provided at time of registration
Publication and dissemination planNot provided at time of registration
IPD sharing plan

Editorial Notes

18/10/2016: No publications found, verifying study status with principal investigator.