The prospective single-arm clinical trial to evaluate safety and efficacy of the training program for esophageal smooth muscle in patients with gastro-esopheal reflux disease.

Not Applicable

• Conditions: gastro-esophageal reflux disease

• Registration Number: JPRN-UMIN000047829
• Lead Sponsor: ishijin Hospital

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2022-05-22
• Last Update Posted: 22 January 2024
• Study Completion: 2024-05-31

Recruitment & Eligibility

• Status: Complete: follow-up continuing
• Sex: All
• Target Recruitment: 20

Inclusion Criteria

Not provided

Exclusion Criteria

Difficulty evaluating their own condition because of dementia or mental disturbance. Heart or respiratory failure, spinal disease or other poor general condition. Disfunction of esophagus, stomach, pharyngolarynx affected by past operation or endoscopic treatment. Pregnancy or breast-feed.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
The numerical value change of FSSG (Frequency Scale for the Symptoms of GERD) in the second week of training implementation.

Secondary Outcome Measures

Name	Time	Method
The numerical value change of FSSG in the 4th or 8th week of training implementation. The quantity of proton pump inhibitor required in the 2nd, 4th, or 8th week of training implementation.