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Analysis of Postoperative Efficacy of Preoperative Pelvic Floor Manual Massage Combined with Low-Frequency Electrical Stimulation Therapy in Patients with Pelvic Organ Prolapse Complicated by Non-Relaxing Pelvic Floor Dysfunction: A Prospective Cohort Study

Analysis of Postoperative Efficacy of Preoperative Pelvic Floor Manual Massage Combined with Low-Frequency Electrical Stimulation Therapy in Patients with Pelvic Organ Prolapse Complicated by Non-Relaxing Pelvic Floor Dysfunction: A Prospective Cohort Study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500104801
Enrollment
Unknown
Registered
2025-06-24
Start date
2025-06-30
Completion date
Unknown
Last updated
2025-06-30

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

Conditions

Pelvic organ prolapse

Interventions

Research Group:Pelvic floor muscle hypertonicity therapy (pelvic floor massage + low-frequency electrical stimulation therapy) is performed before surgery
Control group:No pelvic floor muscle hypertonicity physical therapy intervention was performed before surgery

Sponsors

Obstetrics and Gynecology Hospital of Fudan University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Patients with pelvic organ prolapse quantification (POP-Q) score, II degree or above in any of the anterior, middle and posterior pelvic organ prolapse; 2. Patients with NPFD; 3. Patients who refuse conservative treatment or have failed conservative treatment; 4. Patients willing to undergo surgery; 5. Patients with urinary incontinence; 6. Patients who cooperate with regular follow-up after surgery.

Exclusion criteria

Exclusion criteria: 1. Those who subjectively reject the offered prolapse surgery plan; 2. Patients who have received related treatment for hypertonic pelvic floor dysfunction in the past; 3. Patients with severe internal and external diseases, tumors, infections, and bleeding who are not suitable for surgery; 4. Patients suspected or diagnosed with pelvic malignant tumors.

Design outcomes

Primary

MeasureTime frame
Pelvic floor dysfunction assessment:PFDI-20;

Secondary

MeasureTime frame
Postoperative complications;Recovery status of anxiety and depression;Perioperative evaluation indicators: length of stay, cost of stay, pain VAS score, postoperative exhaust time, incidence of postoperative urinary retention, and incidence of constipation;

Countries

China

Contacts

Public ContactYisong Chen

Obstetrics and Gynecology Hospital of Fudan University

cys373900207@163.com+86 136 0191 3713

Outcome results

None listed

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