A randomized controlled study on the improvement of pelvic floor function by low frequency electrical stimulation after pelvic floor reconstruction

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2000032432

Enrollment

Unknown

Registered

2020-04-28

Start date

2020-05-23

Completion date

Unknown

Last updated

2020-05-11

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

Conditions

Female pelvic floor dysfunction

Interventions

Intervention group: low frequency electrical stimulation

control group:N/A

Eligibility

Sex/Gender

Female

Age

40 Years to 70 Years

Inclusion criteria

Inclusion criteria: The patients were 40-70 years old, underwent pelvic floor reconstruction surgery. The subjects agreed to carry out the study and signed the informed consent.

Exclusion criteria

Exclusion criteria: Patients with uterus preserved during operation; patients who need to be supplemented with systemic chemotherapy, pelvic radiotherapy and hormone replacement therapy after operation; patients who take drugs for urinary incontinence after operation; patients with pacemaker implantation; pregnant or planned pregnant women.

Design outcomes

Primary

Measure	Time frame
pelvic organ prolapse quantitive examination, POP-Q;Electrophysiological parameters of pelvic floor;Urodynamic parameters;Score of pelvic floor related questionnaire;	—

Secondary

Measure	Time frame
Ultrasound evaluation index of pelvic floor;	—

Countries

China

Contacts

Public ContactLyu Aiming

Obstetrics and Gynecology Department, Beijing Hospital; National Center of Gerontology; Institute of Geriatric Medicine, Chinese Academy of Medical Sciences

lvaiming1983@163.com+86 13716633843

Outcome results

None listed

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