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A randomized controlled study of the effects of different catheterization methods on bladder function in patients with neurogenic bladder after spinal cord injury

A randomized controlled study of the effects of different catheterization methods on bladder function in patients with neurogenic bladder after spinal cord injury

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300079235
Enrollment
Unknown
Registered
2023-12-28
Start date
2024-01-10
Completion date
Unknown
Last updated
2024-01-08

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

Conditions

spinal cord injury

Interventions

Free drainage group:The patient will use indwelling catheterization with the catheter always open.
Clamped catheter group:The patient will use indwelling catheterization, and the catheter will be clamped intermittently.
Intermittent catheter group:The patient will use intermittent catheterization.

Sponsors

Xijing Hospital, the First Affiliated Hospital of Air Force Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. 18-70 years old; 2. Patients with diagnosed neurogenic bladder after spinal cord injury who are undergoing indwelling catheterization; 3. Course of spinal cord injury: within 6 months; 4. No cognitive impairment, simple mental state examination (MMSE) score > 23 points; 5. Patients or immediate family members sign informed consent.

Exclusion criteria

Exclusion criteria: 1. Patients with any urinary dysfunction before spinal cord injury; 2. There are complications such as urinary tract infection, abnormal kidney function, and urinary calculi. 3. The following conditions exist: ? complicated urethral or bladder injury (urethral bleeding, hematuria); (2) Abnormal urethral anatomy such as stricture, false passage and bladder neck obstruction; ? Bladder volume less than 200ml; ? Complicated with vesicoureteral reflux and hydronephrosis; (5) Inability or unwillingness to adhere to timed catheterization or limit fluid intake; ? People who have adverse reactions caused by inserting urinary tubes from their genitals several times a day; 4. The presence of an unstable condition or a known uncontrolled systemic disease.

Design outcomes

Primary

MeasureTime frame
Safe bladder capacity;Neurogenic bladder symptoms score;

Secondary

MeasureTime frame
SF-Qualiveen;Residual urine volume;Post-perfusion bladder pressure;Bladder capacity and corresponding bladder pressure at first filling sensation;Bladder volume and corresponding bladder pressure at first urination sensation;Bladder volume and corresponding bladder pressure at intense urination sensation;Bladder volume and corresponding bladder pressure at urgent urination sensation;Successful removal rate of urinary tube;Occurrence of complications;

Countries

China

Contacts

Public ContactHua Yuan

Xijing Hospital, the First Affiliated Hospital of Air Force Medical University

yuanhua@fmmu.edu.cn+86 29 8477 5439

Outcome results

None listed

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