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NCT04682691

Effect of Metoclopramide Versus Erythromycin on on Gastric Residual Volume

Completed NA Last updated 14 January 2025
What this trial tests

NA trial testing Erythromycin (400mg) in Gastric Residual Volume in 50 participants. Completed in 22 February 2024.

Timeline
1 March 2021
Primary endpoint
5 February 2024
22 February 2024

Quick facts

Lead sponsorCairo University
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingquadruple
Primary purposeprevention
Enrollment50
Start date1 March 2021
Primary completion5 February 2024
Estimated completion22 February 2024
Sites1 location across Egypt

Drugs / interventions tested

Conditions studied

Sponsor

Cairo University

Who can join

18 and older, female only, with Gastric Residual Volume. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

In emergencies, it may be necessary to anaesthetize who are not fully starved and consequently at risk of pulmonary aspiration. Pregnancy are recognized to be at increased risk of aspiration compared with non-pregnancy. Prokinetic agents such as metoclopramide can be used to reduce GRV. Metoclopramide is widely used as a prokinetic agent in adults and is licensed for premedication in pregnancy, but its use may be limited by its potential for producing extrapyramidal side effects. Erythromycin is an effective prokinetic agent in adults but there is no work examining its use for premedication in pregnancy. This study compared the effects of erythromycin and metoclopramide on GRV in full-term pregnant women

Publications & conference data

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

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Other recruiting trials for Gastric Residual Volume

Currently open trials in the same condition.

Other Cairo University trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

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