Low Dose Aspirin Studied With the AggreGuide

This study has been completed.
Information provided by (Responsible Party):
Edward R. Teitel, M.D., Aggredyne, Inc.
ClinicalTrials.gov Identifier:
First received: May 21, 2012
Last updated: July 14, 2012
Last verified: July 2012
This study is to determine whether the AggreGuide platelet aggregometer can discern the effect of low dose aspirin on subjects platelet aggregation using arachidonic acid as the agonist.

Platelet Aggregation

Study Type: Observational
Study Design: Observational Model: Case-Crossover
Time Perspective: Prospective
Official Title: Low Dose Aspirin Study With the AggreGuide

Resource links provided by NLM:

Further study details as provided by Aggredyne, Inc.:

Biospecimen Retention:   None Retained
whole blood

Enrollment: 13
Study Start Date: April 2012
Study Completion Date: June 2012
Primary Completion Date: June 2012 (Final data collection date for primary outcome measure)

Ages Eligible for Study:   18 Years to 70 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes
Sampling Method:   Non-Probability Sample
Study Population
community sample

Inclusion Criteria:

  • adults

Exclusion Criteria:

  • aspirin contraindications
  • anticoagulants
  • aspirin past week
  Contacts and Locations
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Please refer to this study by its ClinicalTrials.gov identifier: NCT01603966

United States, Texas
Aggredyne, Inc.
Houston, Texas, United States, 77099
Sponsors and Collaborators
Edward R. Teitel, M.D.
Principal Investigator: Edward R. Teitel, MD Aggredyne, Inc.
  More Information

Responsible Party: Edward R. Teitel, M.D., CEO, Aggredyne, Inc.
ClinicalTrials.gov Identifier: NCT01603966     History of Changes
Other Study ID Numbers: Val-030 
Study First Received: May 21, 2012
Last Updated: July 14, 2012
Health Authority: United States: Institutional Review Board

Keywords provided by Aggredyne, Inc.:

ClinicalTrials.gov processed this record on May 23, 2016