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NCT03968302

ADDITION OF BISMUTH TO THE STANDARD TRIPLE THERAPY FOR HELICOBACTER PYLORI ERADICATION

Completed Phase 2 Last updated 30 May 2019
What this trial tests

Phase 2 trial testing ARM A Triple therapy for helicobacter pylori in Helicobacter Pylori Infection in 196 participants. Completed in 15 May 2019.

Timeline
1 June 2018
Primary endpoint
15 May 2019
15 May 2019

Quick facts

Lead sponsorZiauddin University
PhasePhase 2
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposetreatment
Enrollment196
Start date1 June 2018
Primary completion15 May 2019
Estimated completion15 May 2019
Sites1 location across Pakistan

Drugs / interventions tested

Conditions studied

Sponsor

Ziauddin University

Who can join

Adults 12 to 80, any sex, with Helicobacter Pylori Infection. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

H pylori is an important cause of chronic gastritis and other complications. There is a decline in eradication rate for H pylori owing to multiple factors including drug resistance. We compare the effect of the addition of bismuth to the standard triple therapy in a randomized control trial. Subjects were randomized into two arms. Arm A received triple therapy including amoxicillin, clarithromycin, and omeprazole and Arm B received quadruple therapy adding colloidal bismuth subcitrate. Both arms received treatment for two weeks.

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 Helicobacter Pylori Infection

Currently open trials in the same condition.

Other Ziauddin University trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

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