Deprescribing Inappropriate Proton Pump Inhibitors

Recruiting N/A Interventional Study
Inappropriate Prescribing Reflux Disease Proton Pump Inhibitors
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 and older
Sex
Any
Study type
Interventional
Purpose
Health Services Research
Participants needed
400 (estimated)
Sponsor
University of Bern · Other
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About This Trial
The DROPIT Trial is an interventional, open-labelled, cluster-randomized controlled trial conducted in the Swiss primary care setting. It aims to evaluate an intervention to guide the deprescribing of inappropriate proton-pump inhibitors (PPIs). Therefore, the trial investigates whether the study intervention leads to the deprescribing of inappropriate PPI prescription while ensuring noninferiorit…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: 1. Patient of a participating GP. 2. Age: minimum 18 years old. 3. Daily PPI intake for minimum 8 weeks. 4. PPI in one of the following doses: * minimum 40mg/day pantoprazole; * minimum 40mg/day omeprazole; * more than 30mg/day lansoprazole; * more than 30mg/day dex…
Contacts

Sven Streit, Prof. Dr med. Dr. phil.

+41 31 684 58 75

sven.streit@unibe.ch

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