Neurogenic lower urinary tract dysfunction secondary to stroke
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: (1) Aged between 35 and 90 years (including 35 and 90 years), regardless of gender; (2) Possession of complete clinical and imaging data; (3) Patients experiencing involuntary urination beyond voluntary control or requiring a urinary catheter due to such incontinence, with at least one episode of urinary incontinence per day; (4) Patients requiring a urinary catheter because they are unable to void spontaneously; (5) Patients with stable vital signs, clear consciousness, no significant cognitive or speech impairments, and the ability to cooperate with relevant treatments and examinations as required by the protocol; (6) No recent use of antibiotics or probiotics that significantly affect the microbial flora; (7) No concomitant diseases that significantly affect the microbial flora; (8) Patients who voluntarily understand the study, agree to participate, and sign the Informed Consent Form.
Exclusion criteria
Exclusion criteria: (1) Patients who do not meet the above inclusion criteria; (2) Patients with NLUTD not caused by stroke, or those with a history of urinary dysfunction prior to the onset of stroke; (3) Patients with concomitant organic urinary tract lesions or inflammatory urinary tract reactions; (4) Patients with other serious illnesses or underlying conditions, such as orthostatic hypotension, hepatic or renal insufficiency, severe spinal cord injury, organ diseases and failure (e.g., prostate cancer), or severe infections; (5) Patients with coagulation disorders or a severe tendency to bleed, or those with poor skin sensation or healing capacity; (6) Patients with contraindications to acupuncture or who cannot undergo acupuncture treatment; (7) Patients taking other medications that may interfere with NLUTD treatment; (8) Patients with severe cognitive or psychiatric impairments who are unable to express their intention to urinate; (9) Patients with poor compliance who cannot consistently cooperate to complete treatment and efficacy assessments; (10) Patients with conditions known to significantly alter the structure of the microbiota (e.g., hyperlipidemia, obesity, etc.); (11) Individuals who have recently taken medications, foods, or related health supplements that significantly affect the microbial flora; (12) Individuals who have recently participated in or are currently participating in other clinical trials.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Gut-urinary tract microbiota; | — |
Secondary
| Measure | Time frame |
|---|---|
| neurogenic bladder symptom score; | — |
Countries
China
Contacts
Chengdu University of Traditional Chinese Med