Resistance to Aspirin and/or Clopidogrel Among Patients With PAD.

Sponsor
Aalborg University Hospital (Other)
Overall Status
Completed
CT.gov ID
NCT00262561
Collaborator
Danish Heart Foundation (Other)
263
1
1
24
11

Study Details

Study Description

Brief Summary

263 patients with peripheral atherosclerosis were examined to evaluate the activity of the platelets during the standard treatment, including aspirin. A subgroup of 43 received 600 mg of clopidogrel 2 h before platelet reactivity analysis.

The main hypothesis is that high platelet activity at the beginning of the study is associated with a higher risk of atherothrombosis. Follow up time is 5 years.

Condition or Disease Intervention/Treatment Phase
Phase 4

Detailed Description

Patients with peripheral atherosclerosis are at high risk of atherothrombosis, mainly heart attack and stroke. The medical treatment of these patients include platelet inhibiting drugs, usually aspirin, to reduce the risk of ischemic events. Clopidogrel is another platelet inhibiting drug, which is prescribed less often, primarily because of the high costs compared to aspirin.

Phenomena of 'resistance' to these drugs have been described by numerous investigators. Essentially resistance means that the effect of the drug described is less than expected or missing, as measured by various laboratory methods. We do not know which way resistance is best described, but it has been described that patients who are 'resistant' to either drug are less protected against future heart attacks or strokes.

Main objectives:
  • To measure the activity of platelets in these patients during aspirin treatment.

  • To measure the activity of platelets in a minor population of these patients during clopidogrel treatment.

  • To evaluate the prognostic significance of resistance to aspirin in these patients.

Methods:

Platelet activity is measured by the PFA-100 (Dade Behring) and by traditional turbidimetric aggregation.

Endpoints:

Myocardial infarction, unstable angina, cerebral infarction, transitory cerebral ischaemia, sudden deterioration of symptoms, percutaneous or surgical vascular intervention, amputation, death.

Study Design

Study Type:
Interventional
Actual Enrollment :
263 participants
Allocation:
Non-Randomized
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Diagnostic
Official Title:
Prevalence of Resistance to Aspirin and/or Clopidogrel Among Patients With PAD. Prognostic Significance of Resistance to Aspirin
Study Start Date :
Jan 1, 2006
Actual Primary Completion Date :
Jan 1, 2008
Actual Study Completion Date :
Jan 1, 2008

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Aspirin

All participants get Aspirin, and platelet reactivity measurements are performed.

Drug: Aspirin
The effect of Aspirin on platelet function was assessed.

Outcome Measures

Primary Outcome Measures

  1. Myocardial infarction, Unstable angina, Cerebral infarction, Transitory cerebral ischaemia, Percutaneous or surgical vascular intervention, Sudden deterioration of symptoms, Amputation, Death. [5 years]

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Atherosclerosis of the lower limbs, defined by one of the following criteria: Ankle-Brachial Pressure Index (ABPI)< 0.9, intermittent claudication, ischaemic pain at rest, ischaemic ulcers or gangrene.

  • Age > 18 years

  • For fertile women: Use of safe contraception (intrauterine contraceptive device, the pill, hormonal skin patches, progestogen injections, progestogen implant, vaginal ring)

Exclusion Criteria:
  • Allergy to either Aspirin or Clopidogrel

  • Known bleeding disorder

  • Platelet count < 140 mia/L or > 400 mia/L

  • Intake of NSAID's, SSRI's or Dipyridamol within the preceding 14 days

  • Not radically treated gastrointestinal ulceration within the last 6 month

  • Greater surgical procedures performed within the last 3 month

  • Severe renal disease

  • Severe hepatic disease

  • Breast feeding

  • Pregnancy

Contacts and Locations

Locations

Site City State Country Postal Code
1 Department of Vascular Surgery, Aalborg Hospital Aalborg Denmark 9000

Sponsors and Collaborators

  • Aalborg University Hospital
  • Danish Heart Foundation

Investigators

  • Principal Investigator: Nils Johannesen, MD, Department of Vascular Surgery, Aalborg Hospital

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Esben Hjorth Madsen, M.D., Aalborg University Hospital
ClinicalTrials.gov Identifier:
NCT00262561
Other Study ID Numbers:
  • 2005-003844-68
First Posted:
Dec 7, 2005
Last Update Posted:
Jan 28, 2014
Last Verified:
Jan 1, 2014
Keywords provided by Esben Hjorth Madsen, M.D., Aalborg University Hospital
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jan 28, 2014