Clinical trial to evaluate the effect of intravaginal electrical stimulation on the sexual dysfunction of women with overacive bladder

Mono-center, placebo-controlled, double-blind, randomized trial to evaluate the efficacy and safety of intravaginal electrical stimulation on the sexual dysfunction of women with overactive bladder

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

CRIS

Registry ID

KCT0006420

Enrollment

Registered

2021-08-04

Start date

2021-05-13

Completion date

Unknown

Last updated

2021-08-30

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

Conditions

None listed

Interventions

Medical Device : Device: intravaginal electric stimulation or placebo Frequency: 40Hz, 12minutes 2 times per day, 8weeks, intravaginal insertion

Eligibility

Sex/Gender

Female

Inclusion criteria

Inclusion criteria: 1. Total Female Sexual Function Index, FSFI score = 26 2. Overactive bladder 3. Age between 20 and 75 years

Exclusion criteria

Exclusion criteria: 1. Grade III or higher urogenital prolapse 2. Cardiac pacemaker 3. Pregnant/ planning to become pregnant 4. Cognitive impairment 5. Neurological or psychiatric disease 6. Urinary tract infection

Design outcomes

Primary

Measure	Time frame
Female Sexual Function Index Score	—

Secondary

Measure	Time frame
Overactive bladder symptom score;Adverse event	—

Countries

Korea, Republic of

Contacts

Public ContactWoong Jin Bae

The Catholic University of Korea, Seoul St. Mary's Hospital

bwoong@catholic.ac.kr+82-2-2258-6226

Outcome results