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Clinical Trials/KCT0004156
KCT0004156
Completed
Not Applicable

Endoscopic functional luminal imaging probe to assess esophagogastric junction distensibility for nonerosive reflux disease

Bundang CHA General Hospital0 sites900 target enrollmentTBD

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Diseases of the digestive system
Sponsor
Bundang CHA General Hospital
Enrollment
900
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
September 30, 2018
Last Updated
6 years ago
Study Type
Observational Study
Sex
All

Investigators

Sponsor
Bundang CHA General Hospital

Eligibility Criteria

Inclusion Criteria

  • All patients who were between 15 and 79 years old, with reflux symptoms, and scheduled to undergo a screening gastroscopy and EndoFLIP® were included in this study. According to the results, patients with erosive esophagitis, determined by gastroscopy, were referred to the ERD group, while patients with no erosive esophagitis, but with abnormalities observed over 24\-hour pH monitoring were classified as the NERD group.12 Healthy controls were on no regular medications and had no symptoms of reflux disease, but did have nonspecific symptoms, such as dyspepsia or abdominal discomfort.

Exclusion Criteria

  • (1\) unable to receive a gastroscopy or EndoFLIP®; (2\) unable to provide informed consent; (3\) hemodynamic instability (systolic blood pressure \[SBP] \< 90 mmHg), or if the peripheral oxygen saturation (SpO2\) was 90% in room air, or \< 95% on 2 L/min of oxygen at baseline before the procedure; (4\) psychological problems; (5\) acute severe infection; (6\) evidence of esophageal
  • motility disorder on esophageal manometry.

Outcomes

Primary Outcomes

Not specified

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