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Proton Pump Inhibitor Treatment Stop

Proton Pump Inhibitor Treatment Stop: Discontinuation of Acid-suppressive Medication Among Long-term Users in a Primary Health Care Setting

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00120315
Enrollment
171
Registered
2005-07-15
Start date
2003-12-31
Completion date
2007-03-31
Last updated
2009-10-06

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

Conditions

Dyspepsia

Keywords

dyspepsia, discontinuation, Primary health care, Helicobacter pylori, Proton Pump Inhibitor, Histamine-2-receptor-antagonist

Brief summary

The purpose of this study is to determine how many chronic users of antisecretory medication can stop after a test for a bacteria associated with peptic ulcer disease. This is evaluated in a discontinuation trial.

Detailed description

Background: Testing patients with a Helicobacter pylori (Hp) 13C-urea breath test and treatment with eradication of Hp if positive - test-and-eradicate - have proven as effective and safe as prompt endoscopy for management of dyspeptic patients in a primary health care setting. However, empirical treatment with an ulcer-healing drug is often used in dyspeptic patients, as reflected in a growing proportion of long-term users without known ulcer or gastro-oesophageal reflux disease (GORD). This group of patients contributed to 59% of the total use of acid-suppressive medication in the County of Funen in Denmark in 1997. Aim/purpose: It is our aim to examine the need for continued medication with prescribed, acid-suppressive drugs in primary health care. Our secondary objective is to investigate the profile of symptoms, quality of life, Hp-status, consumption of drugs and use of health care services in the same context. Methods: To conduct a randomised, placebo-controlled, blinded, clinical discontinuation trial, 500 long-term users of acid-suppressive drugs are identified by general practitioners. Long-term use is defined as treatment for more than 2x28 days during a 6-month period. The patients are included with a 13C-urea Hp-breath test and randomised for treatment with PPI or placebo. Hp-positive patients are treated with an Hp-eradication treatment. The patients are followed for 1 year; the primary outcome is the need for open treatment with acid-suppressive medication due to failing symptom relief despite treatment with the randomised project medication. The patients are to fill in a symptom and medication diary every month for periods of 1 week. Questionnaires are to be given to the patients 3 times during the follow-up period. Medication diaries as well as questionnaires have proven useful in similar studies. The main outcome is analysed using Kaplan-Meier survival estimates analysis.

Interventions

DRUGesomeprazole

esomeprazole, original Nexium, 40 mg pills Up to once a day

PROCEDUREHelicobacter pylori c-13 breath test

Breath test done at entry to find Helicobacter pylori

Sponsors

Research Unit of General Practice, Odense
CollaboratorOTHER
University of Southern Denmark
CollaboratorOTHER
The Danish Medical Research Council
CollaboratorOTHER
Apotekerfonden af 1991
CollaboratorOTHER
AstraZeneca
CollaboratorINDUSTRY
Danish College of General Practitioners
CollaboratorOTHER
Odense University Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Use of antisecretory medication for more than 2 months during the last 6 months

Exclusion criteria

* Malignity or severe, competing medical or psychiatric disease * Esophagitis (proven by endoscopy) * Prior complication to peptic ulcer disease * Alarm symptoms * Pregnancy or lactation * Allergy towards esomeprazole * Planned hospitalisation during study period

Design outcomes

Primary

MeasureTime frame
Failure of patient perceived symptom control despite treatment with project medication12 months

Secondary

MeasureTime frame
Quality of life12 months
GPs and patients satisfaction12 months
Helicobacter pylori statusAt enrolement
Resource consumption12 months
Gastrointestinal symptoms12 months
Use of otc-medication12 months
Sick-leave days12 months
Number of visits to primary and secondary healthcare system12 months
Days without symptoms12 months

Countries

Denmark

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 4, 2026