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A clinical study on bionic electrical stimulation combined with Traditional Chinese Medicine for the treatment of postpartum pelvic floor dysfunction.

A clinical study on bionic electrical stimulation combined with Traditional Chinese Medicine for the treatment of postpartum pelvic floor dysfunction.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2025002530
Enrollment
Unknown
Registered
2025-12-24
Start date
2018-09-01
Completion date
Unknown
Last updated
2026-01-12

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

Conditions

Postpartum Pelvic Floor Dysfunction

Interventions

Group ATraditional Chinese Medicine Treatment Group.:Oral taken Traditional Chinese Medicine.
Group B Acupoint Stimulation Group.:Acupoint stimulation
Group C Oral taken of Traditional Chinese Medicine and Acupoint Stimulation Treatment Group.:Oral taken of Traditional Chinese Medicine and Acupoint Stimulation Treatment
Group D Electrical Stimulation Biofeedback Therapy.Electrical Stimulation Biofeedback Therapy:Electrical stimulation and biofeedback therapy

Sponsors

Hangzhou women's hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
25 Years to 35 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: (1) All patients were diagnosed with pelvic organ prolapse and/or stress urinary incontinence upon admission; (2) All patients were first-time full-term singleton deliveries without the use of vaginal assistive devices during labor; (3) Gynecological examinations indicated mild to moderate prolapse of the anterior and posterior vaginal walls, with the distance from the hymenal margin to the cervical external os being less than 4 cm, and three-dimensional pelvic floor ultrasound showed no abnormal residual tissue in the uterus; (4) The study protocol was approved by the hospital's medical ethics committee, and all patients provided informed consent and signed the agreement.

Exclusion criteria

Exclusion criteria: Exclusion criteria: (1) Exclusion of cases caused by urinary tract infections, tumors or surrounding tissue hyperplasia, compression, and neurological disorders; (2) Patients with acute or chronic pelvic inflammatory disease, severe vaginal infections, and gynecological tumors; (3) Patients with severe cardiac, liver, or renal dysfunction who are unable to adhere to treatment; (4) Patients with severe psychological disorders and those with impaired sensory perception dysfunction; (5) Incomplete data and those who cannot adhere to treatment; (6) Patients who refuse to sign the informed consent form.

Design outcomes

Primary

MeasureTime frame
Pelvic Organ Prolapse Quantification;bladder neck-symphyseal distance,BSD;distance between lowest point of uterus and lower edge of pubic symphysis, C-VD;distance between rectal ampulla and lower edge of pubic symphysis, RA-VD;

Secondary

MeasureTime frame
Pelvic Floor Muscle Strength Assessment;Dynamic Vaginal Pressure Assessment;Quantitative Scoring of Traditional Chinese Medicine Syndromes;

Countries

China

Contacts

Public ContactGuo Qingge

Hangzhou women's hospital

guoqingge6@gmail.com15990027112

Outcome results

None listed

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