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Study for Endoscopic pressure study integrated system (EPSIS)

Study for Endoscopic pressure study integrated system (EPSIS) - Study for EPSIS

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000054930
Enrollment
60
Registered
2024-07-10
Start date
2024-08-01
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Gastroesophageal reflux disease

Interventions

Performing EPSIS during upper gastrointestinal endoscopy in patients suspected of having GERD

Sponsors

Tohoku University Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients who suspect GERD and are scheduled to undergo upper gastrointestinal endoscopy and MII/pH monitoring at our hospital.

Exclusion criteria

Exclusion criteria: (1) Have an active infection. (2) Have a heart disease with symptoms. (3) History of uncontrolled mental disorder or central nervous system disorder. (4) Pregnant patients

Design outcomes

Primary

MeasureTime frame
Correlation between EPSIS and 24-hour multichannel impedance pH monitoring test results

Countries

Japan

Contacts

Public ContactRyohei Ando

Tohoku University Hospital Digestive Surgery

r-ando@surg.med.tohoku.ac.jp0227177214

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026