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Study of the effectiveness of mosapride for GERD patients with sleep disorders

Study of the effectiveness of mosapride for GERD patients with sleep disorders - Study of the effectiveness of mosapride for GERD patients with sleep disorders

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000012363
Enrollment
100
Registered
2013-11-20
Start date
2013-11-21
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

Proton pump inhibitor of the standard dose (+) mosapride(15 mg / day for 4 weeks) Proton pump inhibitor of the standard dose(+) Placebo(+)

Sponsors

Department of Gastroenterology , Shimane University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: In GERD patients with sleeping disorders, who Proton pump inhibitor of standard doses of (PPI) during treatment

Exclusion criteria

Exclusion criteria: Example that started the oral sleep-inducing agent within two weeks. Patients with serious underlying disease that affect sleep. Examples are allergic to mosapride. Examples of oral administration of the drug combination and attention mosapride. Examples of oral medicine in the related to gastrointestinal motor function. Patients with psychiatric disorders. Examples of surgical procedures after the gastroesophageal. Example pregnant or nursing. Example not be obtained consent. Example the attending physician is deemed inappropriate.

Design outcomes

Primary

MeasureTime frame
Pre-dose, two weeks after dosing, four weeks after dosing, have them listed Japanese translation of the Quality of Life in Reflux and Dyspepsia (QOLRAD-J), Epworth Sleepness Scale (ESS), Pittsburgh Sleep Quality Index in (PSQI), respectively to evaluate.

Countries

Japan

Contacts

Public ContactEiko Okimoto

Shimane University School of Medicine Department of Gastroenterolog

okimotoeiko@outlook.com0853-20-2190

Outcome results

None listed

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