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The Impact of Preoperative Electrostimulation Biofeedback on the Improvement of Urinary Incontinence and LUTS Symptoms in Patients After Prostate Enlargement Surgery: A Randomized Controlled Trial

The Impact of Preoperative Electrostimulation Biofeedback on the Improvement of Urinary Incontinence and LUTS Symptoms in Patients After Prostate Enlargement Surgery: A Randomized Controlled Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500104989
Enrollment
Unknown
Registered
2025-06-26
Start date
2025-07-01
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

Benign Prostatic Hyperplasia, BPH

Interventions

Control Group:Glazer EMG assessment was performed the day before surgery
Experimental group:2 weeks before surgery, combined with the actual situation of the patient, the treatment plan of electrical stimulation biofeedback was formulated

Sponsors

Peking University First Hospital
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
50 Years to 90 Years

Inclusion criteria

Inclusion criteria: 1. Men with symptoms of dysuria > = 3 months prior to the start of the study; 2. Elective prostate laser enucleation (Thulep); 3. Patients with 200ml>=prostate volume>=30ml; 4. Age 50-90 years old; 5. Patients who can continue to exercise pelvic floor muscles on their own and can cooperate with the completion of biofeedback therapy; 6. Patients who have had their urinary catheter removed before discharge and can urinate on their own.

Exclusion criteria

Exclusion criteria: 1. Have clear manifestations of urine leakage in the past; 2. Failure to perform standard range resection or incomplete surgical records during surgery due to various reasons; 3. Lost to follow-up or incomplete follow-up data; 4. Patients with severe mental disorders with neurogenic bladder and other organic voiding disorders; 5. Patients with severe heart, kidney and other organ lesions; 6. Patients with urethral stricture and obstruction; 7. Those with urinary tract infection and obvious lower urinary tract symptoms.

Design outcomes

Primary

MeasureTime frame
The recovery time of urinary control after surgery.;International Consultation on Incontinence Questionnaire Short Form (ICI-Q-SF) score after surgery;

Secondary

MeasureTime frame
Postoperative International Prostate Symptom Score (IPSS);Postoperative Overactive Bladder Symptom Score (OABSS);Postoperative pelvic floor electromyographic (EMG) data;Postoperative erectile function score (IIEF-5);

Countries

China

Contacts

Public ContactHan Jianing

Peking University First Hospital

hjn666@163.com+86 186 0134 9200

Outcome results

None listed

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