z-logo
Premium
Identifying response to acid suppressive therapy in functional dyspepsia using a random starting day trial – is gastro‐oesophageal reflux important?
Author(s) -
Madsen L. G.,
Wallin L.,
Bytzer P.
Publication year - 2004
Publication title -
alimentary pharmacology and therapeutics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.308
H-Index - 177
eISSN - 1365-2036
pISSN - 0269-2813
DOI - 10.1111/j.1365-2036.2004.02084.x
Subject(s) - medicine , omeprazole , reflux , gastro , placebo , randomized controlled trial , clinical trial , gastroenterology , pathological , disease , pathology , alternative medicine
Summary Background : Single subject trials offer an alternative approach to identify and characterize responders to a specific treatment. Aim : To test a new single subject trials design, called random starting day trial, to identify acid‐related symptoms in dyspepsia. Methods : A total of 119 patients with functional dyspepsia entered a 12‐day, double‐blind random starting day trial. All patients started on placebo and switched to omeprazole 80 mg/day at a randomized and blinded day between day 5 and day 9, with active treatment continuing for the rest of the trial. Based on changes of a daily symptom score, response was defined as a sustained ≥50% reduction of symptoms within 3 days of active treatment. Results : Thirteen of 119 patients (11%) were classified as spontaneous responders because of complete symptom relief before switching to omeprazole. Of the remaining 106 patients, 15 (15.6%) were classified as responders. Five of six (83%) responders compared with 28 of 53 (53%) non‐responders had pathological reflux. Multivariate testing identified symptoms suggestive of gastro‐oesophageal reflux predictive of response. Conclusions : The random starting day trial design could identify a subset of dyspeptic patients with a uniform symptomatic response to acid‐suppressive therapy. Response seems to be associated with gastro‐oesophageal reflux. The random starting day trial needs to be further validated to be considered as a reliable instrument in clinical research.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom