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Comparison of the effectiveness of the three treatment methodes; transecutaneous nerve stimulation by constant parameters, transecutaneous nerve stimulation by variasble parameters and treatment by Solifenacin

Comparison of the effectiveness of the three treatment methodes; transecutaneous nerve stimulation by constant parameters, transecutaneous nerve stimulation by variasble parameters and treatment by Solifenacin

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20190202042581N2
Enrollment
16
Registered
2019-06-20
Start date
2019-07-23
Completion date
Unknown
Last updated
2019-08-26

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

Conditions

Women's urgent incontinence. Urge incontinence

Interventions

Intervention 1: Intervention group: CTTNS group: Tibial nerve stimulation with frequency of 20 Hz and 200 µs duration. Intervention 2: Intervention group: VTTNS group: Initial tibial tibial stimulati

Sponsors

Hamedan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
50 Years to No maximum

Inclusion criteria

Inclusion criteria: Postmenopausal women Age over 50 years Urine excretion at least 8 times a day, based on history or voiding diary ore than once, the episode was an urgency with or without discretion

Exclusion criteria

Exclusion criteria: Sensitivity to sulfenacin or its elements Urinary retention Gastric retention Neuropathy Uncontrolled narrow glaucoma angle

Design outcomes

Primary

MeasureTime frame
Severity of incontinence. Timepoint: At the beginning of the study and 6 weeks after starting treatment. Method of measurement: OABS questionnaire.;Quality of life. Timepoint: At the beginning of the study and 6 weeks after starting treatment. Method of measurement: Quality of Life questionnaire.

Secondary

MeasureTime frame
The frequency of urinary leakage. Timepoint: At the beginning of the study and 6 weeks after starting treatment. Method of measurement: Patient report.;Frequent feelings of urgency. Timepoint: At the beginning of the study and 6 weeks after starting treatment. Method of measurement: Patient report.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactHojat Radinmehr

Hamedan University of Medical Sciences

h.radinmehr@umsha.ac.ir+98 81 3838 1571

Outcome results

None listed

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