Bladder function in patients with overactive bladder after cystocele repair

Evaluation of bladder function in patients with overactive bladder after cystocele repair

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT20201108049307N1

Enrollment

Registered

2020-12-18

Start date

2020-10-22

Completion date

Unknown

Last updated

2021-01-05

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

Intervention group: In this group, patients with overactive bladder underwent cystocele repair. Before, one and six months after the intervention, bladder function is checked..

Eligibility

Sex/Gender

Female

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: Age 18 years and older Diagnosis of overactive bladder Frequent urination more than eight times a day Feeling of urinary urgency more than once a day Being married Satisfaction to participate in the study

Exclusion criteria

Exclusion criteria: Breastfeeding Pregnancy Use of contraceptive methods Anticholinergic contraindication Need for catheter Obstruction of bladder outlet History of genitourinary surgery

Design outcomes

Primary

Measure	Time frame
Urine urgency. Timepoint: Before, 1 month and 6 months after the intervention. Method of measurement: Visual Analogue Scale.;Frequent urination. Timepoint: Before, 1 month and 6 months after the intervention. Method of measurement: Visual Analogue Scale.;Urgent incontinence. Timepoint: Before, 1 month and 6 months after the intervention. Method of measurement: Visual Analogue Scale.;Genital pain. Timepoint: Before, 1 month and 6 months after the intervention. Method of measurement: Visual Analogue Scale.	—

Measure

Time frame

Urine urgency. Timepoint: Before, 1 month and 6 months after the intervention. Method of measurement: Visual Analogue Scale.;Frequent urination. Timepoint: Before, 1 month and 6 months after the intervention. Method of measurement: Visual Analogue Scale.;Urgent incontinence. Timepoint: Before, 1 month and 6 months after the intervention. Method of measurement: Visual Analogue Scale.;Genital pain. Timepoint: Before, 1 month and 6 months after the intervention. Method of measurement: Visual Analogue Scale.

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Countries

Iran (Islamic Republic of)

Contacts

Public ContactShekofeh Gholi Pour

Esfahan University of Medical Sciences

Behnammokhtari630@gmail.com+98 31 3234 6338

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026