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Effectiveness of a Collaborative Deprescribing Intervention of Proton Pump Inhibitors

Effectiveness of a Collaborative Deprescribing Intervention of Proton Pump Inhibitors: A Randomized Controlled Trial in Pakistan

Status
Recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
TCTR
Registry ID
TCTR20260213005
Enrollment
400
Registered
2026-02-13
Start date
2025-12-01
Completion date
Unknown
Last updated
2026-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Proton pump inhibitors are widely used in primary care, without a valid clinical indication. Their inappropriate prolonged use is associated with the risks of adverse effects and healthcare costs. Despite international guidelines on deprescribing, there is limited evidence on structured, collaborative interventions in low-resource settings like Pakistan Proton pump inhibitors adverse effects collaborative interventions , low-resource settings

Interventions

Receives a structured deprescribing intervention through collaboration between general practitioner and pharmacist.,Receives usual care from their GP without structured deprescribing intervention
Experimental Other,No Intervention No treatment
Collaborative Deprescribing Intervention Group,Control arm

Sponsors

Capital University of Science and Technology
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Patients receiving PPIs for at least three months before enrolment. 2. Participant should show Willingness to participate in the study and provide informed consent 3. Access to primary healthcare settings involved in the study

Exclusion criteria

Exclusion criteria: 1. Confirmed diagnosis requiring long term PPI use 2. Pregnant or breastfeeding women were excluded from the study 3. History of severe gastrointestinal bleeding, peptic ulcer perforation, or malignancy

Design outcomes

Primary

MeasureTime frame
Reduction in prescribed PPI dose over a 6-month follow-up. Baseline, 2 months and 4 Month Mann-Whitney U test (or Wilcoxon rank-sum test)

Secondary

MeasureTime frame
Analysis of possible side effects caused by chronic and long-term PPI use. Baseline, 2 months and 4 Month Mann-Whitney U test (or Wilcoxon rank-sum test

Countries

Pakistan

Contacts

Public ContactFarman Khan

Faculty of Pharmacy Capital University of Science and Technology

farmankhan@bs.qau.edu.pk00923319443131

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 10, 2026