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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02181855
Other study ID # atyGERD-X
Secondary ID
Status Recruiting
Phase N/A
First received July 2, 2014
Last updated January 28, 2015
Start date June 2014

Study information

Verified date January 2015
Source Technische Universität München
Contact Simon Nennstiel, Dr. med.
Phone 089-4140-
Email simon.nennstiel@lrz.tum.de
Is FDA regulated No
Health authority Germany: Ethics Commission
Study type Interventional

Clinical Trial Summary

Patients with atypical symptoms of objectified gastroesophageal reflux disease will be treated by full-thickness gastroplication and the effect of this intervention will be measured by questionnaires and clinical diagnostics (for example pH/MII).


Recruitment information / eligibility

Status Recruiting
Enrollment 23
Est. completion date
Est. primary completion date December 2015
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria:

- Age between 18 years and 80 years

- symptomatic, objectified reflux disease (atypical symptoms - Montreal-classification)

Exclusion Criteria:

- Rejection of study-participation,

- Pregnancy

- negative pH-metry / impedance monitoring (non-objectified reflux)

- hiatal hernia bigger than 2 cm or gastroesophageal junction > Hill IV classification

- different potential reasons for atypical symptoms like heterotopic gastric mukosa in the cervikal esophagus

- Achalasia, esophageal spasm

- Presence of contraindications for the interventions

Study Design

Intervention Model: Single Group Assignment, Masking: Open Label


Related Conditions & MeSH terms


Intervention

Procedure:
Full-thickness gastroplication (GERD-X)
Endoscopic full-thickness gastroplication wit the GERD-X device

Locations

Country Name City State
Austria Krankenhaus der Barmherzigen Schwestern Linz, Klinik für Allgemein- und Viszeralchirurgie Linz
Germany Klinikum Ludwigsburg, Klinik für Innere Medizin, Gastroenterologie, Hämato-Onkologie, Diabetologie und Infektiologie Ludwigsburg
Germany Klinikum rechts der Isar der Technischen Universität München, II. Med. Klinik und Poliklinik München Bavaria
Germany Klinikum rechts der Isar der Technischen Universität München, Klinik und Poliklinik für Chirurgie München Bavaria

Sponsors (1)

Lead Sponsor Collaborator
Technische Universität München

Countries where clinical trial is conducted

Austria,  Germany, 

Outcome

Type Measure Description Time frame Safety issue
Primary Reflux Symptom index 3 months No