Actively Recruiting
Electroacupuncture of Different Treatment Frequency in Chronic Urinary Retention Caused by Lower Motor Neuron Lesions
Led by Guang'anmen Hospital of China Academy of Chinese Medical Sciences · Updated on 2024-05-14
100
Participants Needed
1
Research Sites
21 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The aim of this study is to compare the effects of electroacupuncture of different frequency in patients with chronic urinary retention caused by lower motor neuron lesions
CONDITIONS
Official Title
Electroacupuncture of Different Treatment Frequency in Chronic Urinary Retention Caused by Lower Motor Neuron Lesions
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Diagnosed with urinary retention caused by lower motor neuron lesions (e.g., sacral plexus, cauda equina, or sacral cord lesions).
- 18 years or older.
- Baseline post void residuals (PVR) �3e= 150 mL.
- The course of urinary retention �3e= 1 month.
- Having normal bladder sensation.
- Using clean intermittent catheterization (CIC), indwelling catheterization (IC), manual assisted voiding including putting pressure on abdomen, or cystostomy catheterization.
- Signed informed consent and voluntary participation in the study.
You will not qualify if you...
- Having a lower urinary tract obstruction, such as bladder neck contracture, urethral stricture, prostatic hyperplasia, or large urinary stones that can cause obstruction.
- Having any type of malignant tumors not removed.
- Having severe systemic disorders not controlled.
- Having implanted electrodes of cardiac pacemaker, pudendal nerve stimulation, bladder stimulation, or SNM.
- Pregnancy or lactation.
- Electroacupuncture treatment duration < 2 weeks.
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Guang'anmen Hospital, China Academy of Chinese Medical Sciences
Beijing, China
Actively Recruiting
Research Team
Z
Zhishun Liu
CONTACT
M
Min Yang
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
3
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