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.
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