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The feasibility of endoscopic functional luminal imaging probe in reflux disease

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

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CRIS
Registry ID
KCT0004156
Enrollment
900
Registered
2019-07-19
Start date
2017-01-17
Completion date
Unknown
Last updated
2019-08-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

None listed

Sponsors

Bundang CHA General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion 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

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.

Design outcomes

Primary

MeasureTime frame
cross sectional area, distensiblity index

Secondary

MeasureTime frame
Residual LES pressure, 24-hr ambulatory pH monitoring

Countries

Korea, Republic of

Contacts

Public ContactJoo Young Cho

Bundang CHA General Hospital

cjy6695@dreamwiz.com+82-31-780-5302

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Feb 4, 2026