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AggreGuide 325 mg. Aspirin Study for Aspirin Induced Platelet Dysfunction

AggreGuide 325 mg. Aspirin Study for Aspirin Induced Platelet Dysfunction

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01915407
Enrollment
150
Registered
2013-08-02
Start date
2013-04-30
Completion date
2013-07-31
Last updated
2013-08-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Platelet Dysfunction Due to Aspirin Ingestion

Brief summary

To test the AggreGuide A-100 AA Assay's effectiveness for detecting aspirin induced platelet dysfunction.

Interventions

None listed

Sponsors

Aggredyne, Inc.
Lead SponsorINDUSTRY

Study design

Observational model
COHORT
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* over 18

Exclusion criteria

* on aspirin in prior week * medical history of platelet disorders * contraindications to aspirin

Design outcomes

Primary

MeasureTime frameDescription
Platelet Activity Index (PAI) before and after ingestion of aspirin2 - 30 hours post aspirin ingestionPAI is the proprietary reporting unit of the Aggreguide. It is related to the amount of platelet aggregation in the sample of whole blood.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026