Skip to main content
Clinical Trials/ITMCTR2100004962
ITMCTR2100004962
Recruiting
Phase 1

Study on the therapeutic effect of floating needle therapy combined with pressing acupoint embedding for female stress urinary incontinence after childbirth

ingbo City Hospital of Traditional Chinese Medicine0 sitesTBD

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
female stress urinary incontinence
Sponsor
ingbo City Hospital of Traditional Chinese Medicine
Status
Recruiting
Last Updated
3 years ago

Overview

Brief Summary

No summary available.

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

Investigators

Sponsor
ingbo City Hospital of Traditional Chinese Medicine

Eligibility Criteria

Inclusion Criteria

  • 1\.The symptoms were compliance with diagnostic criteria for stress urinary incontinence proposed by the International Urinary Inhibition Advisory Board (International Continence Society) of the International Urinary Control Association ICS), which is to say patients could sneezing or coughing, the involuntary leakage of urine from the external urethral orifice and so on when abdominal pressure increased :
  • (1\)Urinary incontinence was mild SUI when people happened to cough and so on only under the condition of increasing abdominal pressure;
  • (2\)Urinary incontinence was moderate SUI when patients performed during daily activities such as walking and standing up from a chair;
  • (3\)Urinary incontinence was severe SUI while people occurred to urinary incontinence during standing or rest.
  • 2\.Urinary incontinence was confirmed by urodynamic tests; no age limit; women with a history of pregnancy and childbirth; people had complete clinical data; people had history of anuria before birth; people could persist the treatment until the end of the course of treatment and timely follow\-up;
  • 3\.Patients and their families were informed and voluntary to participate project studies and they signed informed consent finally.

Exclusion Criteria

  • 1\.Patients with pelvic floor muscle dysfunction and prenatal severe pregnancy complications;
  • 2\.Previous history of urinary incontinence and pelvic organ prolapse;
  • 3\.Persons with acute inflammation of the urinary system;
  • 4\.The presence of lower urinary tract obstruction;
  • 5\.Complicating serious primary diseases such as cardiovascular, cerebrovascular, liver, kidney and hematopoietic systems;
  • 6\.Increased abdominal pressure due to chronic obstructive emphysema or constipation;
  • 7\.History of vaginitis, pelvic inflammation and urinary tract infection, stones, urinary incontinence;
  • 8\.Urgency urinary incontinence and mixed urinary incontinence;
  • 9\.Persons with mental illness, cognitive impairment or mental retardation.

Outcomes

Primary Outcomes

Not specified

Similar Trials