A prospective, multi-centre, randomised trial comparing low-dose aspirin with low-dose aspirin plus low-intensity oral anticoagulation in the primary prevention of thrombosis in patients positive for antiphospholipid antibodies

ISRCTN ISRCTN81818945
DOI https://doi.org/10.1186/ISRCTN81818945
Protocol serial number K0554
Sponsor Arthritis Research Campaign (ARC) (UK)
Funder Arthritis Research Campaign (UK)
Submission date
04/02/2002
Registration date
04/02/2002
Last edited
08/10/2013
Recruitment status
No longer recruiting
Overall study status
Completed
Condition category
Circulatory System
Prospectively registered
Protocol
Statistical analysis plan
Results
Individual participant data

Plain English summary of protocol

Not provided at time of registration

Contact information

Dr Munther Khamashta
Scientific

Louise Coote Lupus Unit
St Thomas' s Hospital
The Rayne Institute
London
SE1 7EH
United Kingdom

Phone +44 (0)20 7928 9292
Email 106404.2325@compuserve.com

Study information

Primary study designInterventional
Study designRandomised controlled trial
Secondary study designRandomised controlled trial
Scientific title
Study acronymALIAPAS
Study objectivesNot provided at time of registration
Ethics approval(s)Not provided at time of registration
Health condition(s) or problem(s) studiedPrevention of thrombosis
InterventionPatients will be randomised to either low dose (75 mg) aspirin or low-dose aspirin and low international normalised ratio (INR) warfarin
Intervention typeDrug
PhaseNot Specified
Drug / device / biological / vaccine name(s)Aspirin, warfarin
Primary outcome measure(s)

Not provided at time of registration

Key secondary outcome measure(s)

Not provided at time of registration

Completion date01/01/2006

Eligibility

Participant type(s)Patient
Age groupNot Specified
SexNot Specified
Key inclusion criteriaPatients positive for antiphospholipid antibodies
Key exclusion criteriaNot provided at time of registration
Date of first enrolment01/09/2000
Date of final enrolment01/01/2006

Locations

Countries of recruitment

  • United Kingdom
  • England

Study participating centre

Louise Coote Lupus Unit
London
SE1 7EH
United Kingdom

Results and Publications

Individual participant data (IPD) Intention to shareNo
IPD sharing plan summaryNot provided at time of registration
IPD sharing plan

Study outputs

Output type Details Date created Date added Peer reviewed? Patient-facing?
Results article results 01/02/2014 Yes No