Skip to content

Solifenacin and Worship Quality in Muslim Women

Evaluation of the effect of solifenacin treatment for urinary incontinence on prayer quality in Muslim women

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20240504061648N4
Enrollment
38
Registered
2026-05-10
Start date
2026-05-22
Completion date
Unknown
Last updated
2026-06-01

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

Conditions

Overactive bladder. Overactive bladder

Interventions

Solifenacin according to the treatment protocol administered orally, 5 milligrams daily with the possibility of increasing to 10 milligrams if clinically needed and tolerated, for a duration of 12 wee

Sponsors

Tabriz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: Muslim woman Clinical diagnosis of overactive bladder (OAB) Age 18 to 75 years Informed consent Ability to complete questionnaires

Exclusion criteria

Exclusion criteria: Pregnancy Active urinary tract infection Neurological diseases affecting bladder function Concurrent use of interacting drugs or other antimuscarinics Intolerance or drug discontinuation due to adverse effects Failure to complete post-treatment assessment

Design outcomes

Primary

MeasureTime frame
Comparison of overactive bladder (OAB) questionnaire scores after treatment compared to baseline values (pre-treatment). Timepoint: Baseline, 4 weeks and 12 weeks after the intervention. Method of measurement: ICIQ-OAB questionnaire.;Comparison of Incontinence Praying Ability (I-PA) questionnaire scores after the intervention compared to baseline values (pre-treatment). Timepoint: Baseline, 4 weeks and 12 weeks after the intervention. Method of measurement: I-PA questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSakineh Hajebrahimi

Tabriz University of Medical Sciences

ebrahimis@tbzmed.ac.ir+98 41 3334 7054

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Jun 11, 2026