ID

44774

Description

ODM derived from http://clinicaltrials.gov/show/NCT00291746

Lien

http://clinicaltrials.gov/show/NCT00291746

Mots-clés

  1. 06/03/2012 06/03/2012 -
  2. 04/08/2015 04/08/2015 - Martin Dugas
  3. 20/09/2021 20/09/2021 -
  4. 17/11/2021 17/11/2021 -
Détendeur de droits

AstraZeneca

Téléchargé le

17 novembre 2021

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0

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Eligibility Gastroesophageal Reflux NCT00291746

Eligibility Gastroesophageal Reflux NCT00291746

Einschlusskriterien
Alter 18 Jahre bis 79 Jahre
Subjects who seek medical advice at their family doctor (primary care physician) for symptoms thought by the primary care physician to arise from the upper GI tract
The symptoms thought to pertain to the upper GI tract must have been present for at least 4 weeks prior to Visit 1 and to have occurred at least twice a week during that period
The symptoms thought to pertain to the upper GI tract must have been of at least mild severity for a minimum of 3 days during the week prior to Visit 1
Ausschlusskriterien
Upper GI endoscopy performed within a year prior to Visit 1
Previous anti-reflux surgery, surgery for peptic ulcer or any form of upper gastrointestinal resective surgery
Contra-indication to the BravoTM procedure such as subjects with a history of bleeding diathesis, strictures anywhere along the GI-tract, esophageal varices, obstructions, or subjects equipped with a pacemaker, an implantable cardiac defibrillator or an implantable neurostimulator (NB: subjects with severe esophagitis (grade D) confirmed by endoscopy at Visit 2 can continue the study without performing the BravoTM procedure)
Medizinische Konzepte

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