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STOpping PPI Therapy in Inactive IBD Study (STOP-IT): A Feasibility Study

Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 4
SUMMARY

To investigate the feasibility of proton pump inhibitor (PPI) withdrawal in inflammatory bowel disease (IBD); the data collected will provide valuable information to inform a future multi-centre randomised controlled trial. Evidence suggests that patients with IBD taking PPIs respond less well to medication and require hospital treatment more frequently than patients not taking PPIs. This may be due to changes in the gut microbiota associated with PPI use. A future definitive trial is planned to investigate clinical outcomes in patients who stop PPIs compared with those who continue PPIs, in order to determine the safety implications of PPI use in IBD. However, several uncertainties remain which require investigation before such a trial can be undertaken. It is currently unknown how many patients with IBD take PPIs, how many can successfully stop taking PPIs, how many would be willing to stop treatment, and how many would remain off treatment long term. In some cases, withdrawal of PPIs may result in a short-term increase in acid reflux symptoms. The willingness of patients to participate in such a study is also unknown. This study will be conducted in GP practices, a setting in which IBD trials have not previously been undertaken. The study will recruit 80 participants with IBD aged 16 years and over who have been taking PPIs regularly for more than six months. Half of participants will be randomised to discontinue PPI therapy. Participants will be followed up for 12 months. The study will provide information regarding recruitment rates within GP practices, optimal methods for PPI withdrawal, and whether stopping PPIs affects IBD outcomes.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 16
Healthy Volunteers: f
View:

• Aged 16 years or older.

• An IBD diagnosis as defined through SNOMED codes in primary care databases \[Appendix 5\]

• Taking a PPI regularly for \>6 months prior to enrolment

• Patient-confirmed compliance with PPI therapy (\>75% of prescribed doses)

• Able to give full, independent valid Informed consent

• Stable disease as defined by no change in medication or IBD-related surgery for the last 3 months.

Locations
Other Locations
United Kingdom
University of Nottingham
RECRUITING
Nottingham
Contact Information
Primary
Gordon W Moran, MD, PhD
Gordon.moran@nottingham.ac.uk
0115 9249924
Time Frame
Start Date: 2026-07-01
Estimated Completion Date: 2027-07-01
Participants
Target number of participants: 80
Treatments
Experimental: Continue PPI Therapy
Continue PPI Therapy
Experimental: Withdraw PPI Therapy
Sponsors
Leads: University of Nottingham

This content was sourced from clinicaltrials.gov