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

S

Sheba Medical Center

Status and phase

Unknown
Phase 3

Conditions

Platlet Aggregation
Major Bleeding Outcomes

Treatments

Drug: clopidogrel by chewing
Drug: Placebo

Study type

Interventional

Funder types

Other

Identifiers

NCT00889044
SHEBA-08 -5397-SM-CTIL

Details and patient eligibility

About

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.

Enrollment

30 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Male and Female older than 18 years old with non-ST myocardial infarction

Exclusion criteria

  • Current treatment with anticoagulation medication, any type of cerebro vascular event in the past, active bleeding, active peptic ulcer disease, pregnant women, any inability to sign an informed consent of participate in the study

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Single Group Assignment

Masking

Quadruple Blind

30 participants in 2 patient groups, including a placebo group

clopidogrel by chewing
Experimental group
Treatment:
Drug: clopidogrel by chewing
Placebo
Placebo Comparator group
Treatment:
Drug: Placebo

Trial contacts and locations

2

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Data sourced from clinicaltrials.gov

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