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A randomized controlled study on the recovery of bladder function in patients with neurogenic bladder through autonomous bladder function training

Clinical application of autonomous bladder function training technology in the management of neurogenic bladder

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500115185
Enrollment
Unknown
Registered
2025-12-23
Start date
2023-09-05
Completion date
Unknown
Last updated
2026-01-05

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

Conditions

Neurogenic bladder

Interventions

Control group:Carry out routine rehabilitation care. According to the actual situation of the patient, actively communicate and exchange with them, guide their negative psychological state, explain to
Experimental Group:Strengthen autonomous bladder function training on the basis of routine rehabilitation care

Sponsors

West China Hospital of Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Patients are all over 18 years old; 2. Meet the comprehensive classification criteria for upper/lower urinary tract dysfunction in patients with neurogenic bladder ; 3. All patients have varying degrees of bladder function, and at least one of the following conditions exists: a. The residual urine volume during spontaneous urination exceeds 100ml; b. Urinary incontinence; c. Urinary retention; 4. The patient provides informed consent and is willing to cooperate.

Exclusion criteria

Exclusion criteria: 1. Those with severe acid-base imbalance, water and electrolyte disorder, and severe damage to the functions of organs such as the heart and lungs; 2. Those with severe urinary system infections, bleeding and coagulation disorders, or infectious diseases; 3. Those who have a history of severe heart, liver or kidney diseases, or have undergone major urinary system surgeries such as anterior urethral sphincterotomy or cystostomy; 4. Those with a safe bladder capacity of less than 100ml or bladder perforation; 5. Those with frequent autonomic hyperreflexia (AD), bladder pressure persistently above 40cmH2O, and vesicoureteral reflux; 6. People with consciousness disorders or mental illnesses; 7. Those with unstable conditions; 8. Massive fluid replacement; 9. Those who are unwilling to sign the informed consent form.

Design outcomes

Primary

MeasureTime frame
Urodynamic examination indicators;Urinalysis;Urination Diary;Urinary system ultrasound;

Secondary

MeasureTime frame
Quality of Life Assessment Scale;Satisfaction;

Countries

China

Contacts

Public ContactYang Yue

West China Hospital of Sichuan University

m15982249923@163.com+86 28 8629 8031

Outcome results

None listed

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