Clinical trial for improving the quality of life of female patients with stress urinary incontinence treated by long needle penetrating

Not Applicable

Completed

• Conditions: Stress urinary incontinence

• Registration Number: ITMCTR1900002400
• Lead Sponsor: Shanxi University of Chinese Medicine

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 20 February 2023

Recruitment & Eligibility

• Status: Completed
• Sex: Female
• Target Recruitment: Not specified

Inclusion Criteria

(1) Female aged 30 to 70 years;
(2) Meet the diagnostic standard of stress urinary incontinence;
(3) attending this experiment voluntarily.

Exclusion Criteria

(1) with other type of urinary incontinence;
(2) combing with urine system infection;
(3) with the history of Pelvic reconstructive surgery and SUI surgery;
(4) combing with diabetes, cauda equine syndrome and spinal cord problems;
(5) taking adrenal hormone related medicine;
(6) with peacekeeper or sensitive to mental materials;
(7) with pregnancy or in nursing period;
(8) attending other trials;
(9) other reasons.

Study & Design

• Study Type: Interventional study
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
I-QOL;

Secondary Outcome Measures

Name	Time	Method
72h urine diary card;1 hour pad;