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Completed

NCT Number: NCT00120315

Proton Pump Inhibitor Treatment Stop

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.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

Department of Medical Gastroenterology, Odense University Hospital

Odense, DK-5000, Denmark

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Esomeprazole

Drug

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

Helicobacter pylori c-13 breath test

Procedure

Breath test done at entry to find Helicobacter pylori

Primary outcomes

  1. Failure of patient perceived symptom control despite treatment with project medication

    Time frame: 12 months

Secondary outcomes

  1. Gastrointestinal symptoms

    Time frame: 12 months

  2. Quality of life

    Time frame: 12 months

  3. GPs and patients satisfaction

    Time frame: 12 months

  4. Helicobacter pylori status

    Time frame: At enrolement

  5. Resource consumption

    Time frame: 12 months

  6. Days without symptoms

    Time frame: 12 months

  7. Use of otc-medication

    Time frame: 12 months

  8. Sick-leave days

    Time frame: 12 months

  9. Number of visits to primary and secondary healthcare system

    Time frame: 12 months

Sponsors and collaborators

Lead sponsor

Odense University Hospital

Other

Collaborators

  • Apotekerfonden af 1991
  • AstraZeneca
  • Danish College of General Practitioners
  • Research Unit of General Practice, Odense
  • The Danish Medical Research Council
  • University of Southern Denmark

Registry information

Official study title

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

Important dates

Study start
2003
Primary completion
2007
Study completion
2007
First posted
Jul 15, 2005
Registry last updated
Oct 6, 2009

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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