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NCT03388463

Single Dose Omeprazole Versus High Dose in High-risk Critically Ill Patients.

Completed NA Last updated 3 January 2018
What this trial tests

NA trial testing Omeprazole in Critical Illness in 110 participants. Completed in 17 September 2017.

Timeline
11 May 2016
Primary endpoint
14 August 2017
17 September 2017

Quick facts

Lead sponsorMenoufia University
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designcrossover
Maskingquadruple
Primary purposeprevention
Enrollment110
Start date11 May 2016
Primary completion14 August 2017
Estimated completion17 September 2017

Drugs / interventions tested

Conditions studied

Sponsor

Menoufia University

Who can join

Adults 21 to 70, any sex, with Critical Illness. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Upper gastrointestinal (GIT) bleeding is common in high risk critically ill patients. Hyperacidity has been identified as one of the main reasons for bleeding.1 2 Antacids with different treatment modalities have been studied to establish the best regimen for prophylaxis against bleeding.3 4 Proton pump inhibitors (PPI) are the most common drugs used in the medical field as antacids. The present study was carried out to investigate the beneficial effects of high dose omeprazole versus standard low dose as a prophylaxis against upper GIT bleeding in high risk critically ill patients.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Other trials of Omeprazole

Trials testing the same drug.

Other recruiting trials for Critical Illness

Currently open trials in the same condition.

Other Menoufia University trials

Trials by the same sponsor.

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Data sources for this page

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