Skip to content

Comparison of the treatment effects with laser and biofeedback on overactive bladder syndrome.

A Clinical trial to compare the effect of CO2 laser and biofeedback therapy on quality of life in patients with overactive bladder syndrome.

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016052127998N1
Enrollment
60
Registered
2017-04-04
Start date
2016-05-21
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Overactive Bladder Syndrome. Other specified disorders of bladder

Interventions

Intervention 1: Intervention group1: The patients in the laser group were treated with fractional CO2 laser during three sessions with one-month interval between each two sessions. Intervention 2: Int
Treatment - Drugs
Intervention group1: The patients in the laser group were treated with fractional CO2 laser during three sessions with one-month interval between each two sessions.
Intervention group2: Patients in the biofeedback group were treated twice a week, for 4 weeks. The intervention in this group was pelvic exercise and observing pelvic feedback.

Sponsors

Vice Chancellor for Research, Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
50 Years to 75 Years

Inclusion criteria

Inclusion criteria: Inclusion Criteria: Age more than 50 years; presence of clinical diagnosis for overactive bladder; urgent or mixed incontinence; frequency of urination more than 8 times during the day; urination more than once at night. Exclusion Criteria: absence of patient satisfaction; use of the other treatment during past 3 months; stage 3 or 4 of pelvic floor prolapse; vaginal lesions; use of previous Isoteritinoin; abnormal Pap smear; Diabetes; BMI more than 30.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Urinary frequency. Timepoint: one month after treatment. Method of measurement: Questionnaire.;Urge incontinence. Timepoint: one month after treatment. Method of measurement: Questionnaire.

Secondary

MeasureTime frame
Quality of Life. Timepoint: one month after treatment. Method of measurement: The quality of Life Questionaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr.Maryam Hajhashemy

Pelvic Clinic of Valiasr Hospital

hajhashemy73@yahoo.com+98 21 6658 1616

Outcome results

None listed

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