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Trials / Completed

CompletedNCT01061034

Pharmacological Study That Measures Omeprazole Effect on Aspirins Absorption in Healthy Volunteers

The Effect of Proton Pump Inhibitor (Omeprazole) on Acetosalisylic Acid Absorption.

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
9 (actual)
Sponsor
Assaf-Harofeh Medical Center · Other Government
Sex
All
Age
18 Years – 60 Years
Healthy volunteers
Not accepted

Summary

Aspirin is a weak acid that crosses the gastric and intestinal mucosa by passive diffusion while in its lipophilic nature.Omeprazole, a proton pump inhibitor, inhibits gastric acid secretion. We assumed that omeprazole inhibits aspirin absorption, thus reducing its action on platelets. healthy volunteers, with no known peptic disease or bleeding disorders will be enrolled. All volunteers will receive 7 days of Aspirin (100mg) alone, followed by 14 days of Aspirin and Omeprazole 20mg twice daily for 3 days and then 20mg once daily. Blood levels of Aspirin will be determined by High performance liquid chromatography (HPLC), 0, 1, 2, 4, 6, 10, 24 hours after the administration of Aspirin alone on day 7 and Aspirin plus Omeprazole on day 21. Platelet function tests will be determined by platelet-rich plasma aggregometry in response to Arachidonic acid (500mg/ml), Ristocetin (1.5mg/ml) and Adenosine 5'-diphosphate (20mM) on day 0 as baseline and on day 7 and 21 of the study.

Conditions

Interventions

TypeNameDescription
DRUGaspirin and omeprazoleaspirin 100 mg, once daily aspirin 100 mg and omeprazole 20 mg both once daily.

Timeline

Start date
2007-03-01
Primary completion
2007-06-01
Completion
2007-06-01
First posted
2010-02-02
Last updated
2010-02-02
Results posted
2010-02-02

Locations

1 site across 1 country: Israel

Source: ClinicalTrials.gov record NCT01061034. Inclusion in this directory is not an endorsement.