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NCT00889044

Chewing Clopidogrel in Addition to Regular Oral Clopidogrel Treatment to Improve Platelets Aggregation in Patient With NON ST ELEVATION MI

Status unknown Phase 3 Last updated 26 April 2009
What this trial tests

Phase 3 trial testing clopidogrel by chewing in Platlet Aggregation in 30 participants. Status unknown.

Timeline
1 April 2009
Primary endpoint
1 December 2010
1 June 2011

Quick facts

Lead sponsorSheba Medical Center
PhasePhase 3
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationrandomized
Designsingle group
Maskingquadruple
Primary purposetreatment
Enrollment30
Start date1 April 2009
Primary completion1 December 2010
Estimated completion1 June 2011
Sites2 locations across Israel

Drugs / interventions tested

Conditions studied

Sponsor

Sheba Medical Center

Who can join

18 and older, any sex, with Platlet Aggregation or Major Bleeding Outcomes. Patients with the condition only — healthy volunteers not accepted.

What's being measured

Primary outcomes are the specific endpoints the trial is designed to prove or disprove.

Sponsor's own description

Since the absorption of clopidogrel through the gastrointestinal tract is limited, we want to examine whether adding clopidogrel by chewing will overcome the limited gastrointestinal absorption, and hence will improve the prevention of platelet aggregation.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other Sheba Medical Center trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

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