neurogenic bladder
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: (1) Patients aged 18-75 years with neurogenic bladder (including boundary values), regardless of gender; (2) Voluntarily sign a written informed consent; (3) Able to communicate well with the investigator and willing to comply with the requirements of the entire experiment
Exclusion criteria
Exclusion criteria: (1) Patients with low bladder compliance (less than 20ml/cmH2O) during urodynamic examination; (2) Patients with mechanical obstruction of outflow tract; (3) Patients with complete spinal cord injury; (4) symptomatic urinary infection; (5) Patients with hydronephrosis or vesico-ureter reflux; (6) Patients with renal insufficiency (blood creatinine greater than 1.5 times the upper limit of normal); (7) Bladder and prostate cancer patients; (8) Patients with implanted pacemakers or defibrillators; (9) Senile dementia, brain atrophy, acute phase of cerebrovascular disease, cognitive impairment (10) Epilepsy, mental disorders can not cooperate with the doctor; (11) Patients who are positive for infectious disease screening before surgery (hepatitis B surface antigen, hepatitis C antibody, syphilis antibody and HIV antibody); (12) Pregnant women or patients trying to become pregnant; (13) Participants who participated in other clinical trials 3 months before the trial; (14) Other situations in which the researcher considers it inappropriate to participate in the study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Change in urination frequency from baseline;Frequency of urgent urination;American Urological Association Symptom Index,AUA-SI;Residual urine volume change;Maximum urine flow rate; | — |
Secondary
| Measure | Time frame |
|---|---|
| Nocturia frequency;Frequency of urinary incontinence;Volume of urine per discharge;Patient Perception of Bladder Condition- Scale, PPBC-S;quality of life;neurogenic bowel dysfunction;Intermittent catheterization times;Proportion of patients completely disengaged from intermittent catheterization;The incidence of adverse events; | — |
Countries
China
Contacts
China Rehabilitation Research Center,Beijing Boai Hospital