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To study whether the change of urine osmotic pressure after administration of imidafenacin for over active bladder patients with nocturia could be the prediction of its antidiuretic effectiveness.

To study whether the change of urine osmotic pressure after administration of imidafenacin for over active bladder patients with nocturia could be the prediction of its antidiuretic effectiveness. - The antidiuretic effectiveness of imidafenacin for patients with nocturia

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCT1091220405
Enrollment
80
Registered
2019-01-17
Start date
2019-11-01
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

over active bladder

Interventions

Intervention type:DRUG Name of intervention:imidafenacin Dose form / Japanese Medical Device Nomenclature:TABLET Route of administration / Site of application:ORAL Dose per administration:0.1 mg Dosin

Sponsors

Department of Urology, Kindai University Faculty of Medicine, Osaka-Sayama, Japan
Lead Sponsor
Department of Urology, Faculty of Medicine, Kindai University Nara Hospital, Ikoma, Japan Department of Urology, Mimihara General Hospital, Sakai, Japan
Collaborator

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: over active bladder patients with nocturia

Exclusion criteria

Exclusion criteria: the patients with acute urinary tract infections, urinary retention, closed angle glaucoma,severe heart failure, using anticholinergic agents, beta-3stimulator, urethral and ureteral catheter

Design outcomes

Primary

MeasureTime frame
urine osmotic pressure

Secondary

MeasureTime frame
IPSS, OABSS, urine osmotic pressure, urinary flow, residual urine volume, nocturnal polyuria index, sodium and creatinine level of casual urine specimen

Countries

Japan

Contacts

Public ContactMamoru Hashimoto

Kindai University, Faculty of Medicine

hashimot@med.kindai.ac.jp+81-72-366-0221

Outcome results

None listed

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