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Clinical Trials/KCT0003912
KCT0003912
Recruiting
未知

Efficacy and Safety of Electroacupuncture and Acupuncture in Postmenopausal Women with overactive bladder ; A multicenter, randomized, controlled, parallel clinical trial

Dongguk University Ilsan Oriental Hospital0 sites147 target enrollmentTBD

Overview

Phase
未知
Intervention
Not specified
Conditions
Diseases of The genitoruinary system
Sponsor
Dongguk University Ilsan Oriental Hospital
Enrollment
147
Status
Recruiting
Last Updated
6 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
6 years ago
Study Type
Interventional Study
Sex
Female

Investigators

Sponsor
Dongguk University Ilsan Oriental Hospital

Eligibility Criteria

Inclusion Criteria

  • The inclusion criteria for the study will be as follows: (1\) women over 40 years of age without the possibility of pregnancy; (2\) those who have a history of amenorrhea for at least 1 year and have no previous history of hormone replacement therapy for the last 6 months; (3\) those who have symptoms of urinary frequency and urgency lasting more than 3 months; (4\) those who fit the diagnostic criteria for OAB, with a total score of more than 3 points on the Korean version of the Overactive Bladder Symptom Score (OABSS); (5\) those who have an average urinary frequency of more than eight times per day and urgency defined by the urgency rating scale (URS) on the bladder diary of more than 2 points and/or urgent urinary incontinence (UUI) on the 3\-day bladder diary during a 1\-week screening period; (6\) those who agree to this clinical study after sufficient explanation.

Exclusion Criteria

  • The exclusion criteria for the study are as follows: (1\) diagnosed with UTI by urine examination; (2\) having stress urinary incontinence without symptoms of OAB; (3\) suspected of having voiding dysfunction induced by neurological damage; (4\) a medical history of cystocele, uterine prolapse or similar condition; (5\) a medical history of obstructive uropathy such as urinary stones and urinary tumors; (6\) a surgical history of urethra or bladder; (7\) a medical history of malignant tumors of the urinary tract; (8\) a medical history of neurological disease or psychiatric illness; (9\) an artificial cardiac pacemaker or implantable cardioverter defibrillator in the chest; (10\) having experienced a hypersensitivity reaction after an acupuncture treatment, or showing any other contraindications; (11\) having participated in another clinical trial within the past three months; (12\) having taken therapeutic drugs that may affect bladder function within one month of the start of this study; (13\) having inadequate literacy to complete the study documents.

Outcomes

Primary Outcomes

Not specified

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