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Study investigating the prevalence of primary insomnia responsive to proton pump inhibitor treatment

Study investigating the prevalence of primary insomnia responsive to proton pump inhibitor treatment - proton pump inhibitor treatment for primary insomnia

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000003626
Enrollment
200
Registered
2010-05-24
Start date
2010-05-01
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

primary insomnia

Interventions

Administration of 20mg/day omeprazole placebo

Sponsors

Department of Gastroenterology and Hepatology, Shimane University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients who need administration of a sleeping medicine for the treatment of insomnia.

Exclusion criteria

Exclusion criteria: Usage of a sleeping medicine in 2 weeks. Cases treated as mental illness. Usage of PPI or H2RA in 2 weeks. With diseases that may influence sleep. Pregnant or lactating women. With allergy to omeprazole etc. Others which attending doctors decide not suitable.

Design outcomes

Primary

MeasureTime frame
Canges of QOLRAD-J, ESS, PSQI

Countries

Japan

Outcome results

None listed

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