Skip to content

Clinical Study on Treatment of Neurogenic Bladder by Electroacupuncture on Ba Liao Point Under Ultrasound Guidance

Clinical Study on Treatment of Neurogenic Bladder by Electroacupuncture on Ba Liao Point Under Ultrasound Guidance

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05447247
Enrollment
114
Registered
2022-07-07
Start date
2022-06-01
Completion date
2023-12-30
Last updated
2023-06-18

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

Conditions

To Investigate the Clinical Effect of Acupuncturing Ba Liao for Neurogenic Bladder Under the Guidance of Ultrasound

Brief summary

To explore acupuncture under the premise of real-time, dynamic and accurate positioning of Ba liao point with ultrasound, observe the clinical efficacy of treating neurogenic bladder, clarify the essence of acupoints, and provide a new method for the standardization of acupuncture and moxibustion.

Interventions

OTHERAcupuncturing Ba Liao point under ultrasound guidance

Acupuncturing Ba Liao point under ultrasound guidance

Sponsors

Qilu Hospital of Shandong University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

1. The diagnosis of neurogenic bladder conforms to the main points; 2. Symptoms and signs: patients with lower urinary tract dysfunction such as frequency of urination, urgency of urination, inadequacy of urine or retention of urine, urinary incontinence; Physical examination showed paresthesia in perineum and saddle area. 3. Auxiliary examination; Routine urine examination, B - ultrasonography of urinary system and urodynamic examination. 4. Indwelling catheter has been removed; 5. Conscious and able to accurately express symptoms and signs; 6. Patients who inform patients and their families of the research situation in detail and obtain their consent for treatment. \-

Exclusion criteria

1. Lower urinary tract dysfunction caused by non-nervous system factors such as urethral calculi and organic obstruction; 2. patients with serious heart and lung diseases, liver and hematopoietic diseases and mental diseases; 3. patients with prostate cancer, urethral stricture, bladder neck fibrosis, interstitial cystitis, glandular cystitis and other diseases; 4. patients implanted with urethral stents or sacral nerve electrodes; 5. pregnant and lactation women; 6. Fear of acupuncture, needle-sickness and blood sickness. -

Design outcomes

Primary

MeasureTime frameDescription
Urodynamic studyOnce every two weeks:Before treatment, two weeks after treatment, four weeks after treatmentResidual urine volume, maximum urine flow rate, average urine flow rate, urination time, urine flow time and urine flow rate were assessed
Neurogenic bladder symptom scoreOnce every two weeks:Before treatment, two weeks after treatment, four weeks after treatment.followed up for 3 months after treatmentPatients were evaluated for neurogenic bladder symptoms

Countries

China

Contacts

Primary ContactYijun Du, Master
duyijun.19871006@163.com+86-18560083602

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026