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Clinical Trials/NCT03299985
NCT03299985
Completed
Not Applicable

Effects of Diaphragmatic Myofascial Release in Gastroesophageal Reflux Disease

Cardenal Herrera University1 site in 1 country30 target enrollmentOctober 5, 2017

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Gastroesophageal Reflux Disease
Sponsor
Cardenal Herrera University
Enrollment
30
Locations
1
Primary Endpoint
GERD symptoms
Status
Completed
Last Updated
7 years ago

Overview

Brief Summary

This study is a double blinded randomized clinical trial with two arms which aims to study the effects of diaphragmatic myofascial release in patients with gastroesophageal reflux disease (GERD).

GERD has become in the last decades a common disease at the occidental world affecting between 10 to 15% of this population. That implies a high socio-health cost and the decline of the quality of life of those patients.

The diaphragm muscle surrounds the lower esophageal sphincter, and helps to prevent gastroesophageal reflux. If one or both structures become incompetent, it may appear GERD. Until the moment, the treatment for GERD begins by lifestyle modification, and if it fails, the treatment becomes medical and, in selected cases, surgical.

It exists some studies that have demonstrate that diaphragmatic breathing training can have a positive effect in GERD and the need of drug usage. But until the moment, the effects of a myofascial release of the diaphragm haven't been explored on these patients.

Thirty patients with GERD referred from different hospitals of Valencia will be randomized into two groups:

  • Intervention with myofascial release for the diaphragm
  • Sham treatment group which is going to receive the same number of session treatments with the same manual techniques, but without the myofascial stimulus The protocol that will be applied consists of 4 identical sessions of myofascial release techniques aimed to normalize the myofascial tension of the diaphragmatic muscle. These sessions will be distributed in two weeks.

The study focuses on the analysis of the following variables:

  • Frequency and intensity of the symptoms of GERD: Reflux Disease Questionnaire (RDQ)
  • Specific quality of life for gastrointestinal disease: Gastrointestinal Quality of life Index (GIQLI)
  • Drug usage: weekly milligrams usage of proton pomp inhibitors (PPI) The results of these pre-intervention and post-intervention variables will be compared between the two groups at baseline (first session), at week 3 and at week 6.
Registry
clinicaltrials.gov
Start Date
October 5, 2017
End Date
March 15, 2018
Last Updated
7 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Cardenal Herrera University
Responsible Party
Principal Investigator
Principal Investigator

Juan F. Lisón Párraga, Dr

Head of medicine department

Cardenal Herrera University

Eligibility Criteria

Inclusion Criteria

  • Patients with the diagnostic of GERD

Exclusion Criteria

  • hiatal hernia \>2 cm
  • previous operation at the LES
  • actual erosive esophagitis
  • Congenital or acquired immune disorders.
  • Allergic status of any kind.
  • Systemic diseases (rheumatic, infectious conditions, febrile state, vascular alterations, endocrine including diabetes, metabolic and neoplastic).
  • Leukemia.
  • Severe psychiatric disorders.
  • Neuromuscular or neurological injuries.
  • Aneurysms.

Outcomes

Primary Outcomes

GERD symptoms

Time Frame: 6 weeks

Frequency and intensity of GERD symptoms measured by the Reflux Disease questionnaire (RDQ)

Secondary Outcomes

  • Drug Usage(6 weeks)
  • Specific quality of life for gastrointestinal disease(6 weeks)

Study Sites (1)

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