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Effectiveness and Safety of Vibegron in Patients with Overactive Bladder: A Retrospective Chart Review of Patient Outcomes

Effectiveness and Safety of Vibegron in Patients with Overactive Bladder: A Retrospective Chart Review of Patient Outcomes - Effectiveness and Safety of Vibegron in Patients with Overactive Bladder: A Retrospective Chart Review of Patient Outcomes

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000037233
Enrollment
100
Registered
2019-07-02
Start date
2019-07-02
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

overactive bladder

Interventions

None listed

Sponsors

Nishino Clinic, Koseikai Medical Corp.
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients over 20 years who met the all following criteria; 1) Patients who treated with vibegron over 4 weeks for OAB during November, 2018 to June, 2019. 2) Patients who collected OABSS at the start of vibegron and 4 weeks later.

Exclusion criteria

Exclusion criteria: Nothing

Design outcomes

Primary

MeasureTime frame
The change in Overactive Bladder Symptom Score (OABSS) total score from baseline to 4 weeks

Secondary

MeasureTime frame
1) Change in OABSS sub-scores (4 elements) from baseline 2) Change in International Prostate Symptom Score (IPSS) total score from baseline 3) Change in IPSS sub-scores (3 and 7 elements) from baseline 4) Change in IPSS-QOL score from baseline 5) Proportion of subjects with minimum changes in OABSS total score 6) Individual scores of King's Health Questionnaire (KHQ) 7) Subgroup analyses for OABSS, IPSS, IPSS-QOL, and KHQ

Countries

Japan

Contacts

Public ContactRirei Araiya

Mebix, Inc. Clinical Research Division

vibegron-retro@mebix.co.jp03-4362-4504

Outcome results

None listed

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