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"Effect of Cupping Method in treatment of Urinary incontinence"

Evaluation of the Efficacy of Cupping Method on Urinary Incontinence in Women: A Randomized Clinical Trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20190527043729N2
Enrollment
76
Registered
2021-11-21
Start date
2021-11-22
Completion date
Unknown
Last updated
2021-11-29

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

Conditions

Condition 1: Urge Incontinence. Condition 2: Mixed Incontinence. Urge incontinence Mixed incontinence

Interventions

Intervention 1: Intervention group is treated with Static Hot Dry Cupping, With flaming alcohol cotton, a vacuum is created in each cup so that the cup sticks to the skin. The skin should protrude 2 t

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
30 Years to 70 Years

Inclusion criteria

Inclusion criteria: 30-70 Old Women with Urge or Mixed urinary Iincontinence; Being symptomatic for at least 3 months; Not been treated for at least 2 week before study

Exclusion criteria

Exclusion criteria: Acute or Recurrent Urinary Tract Infection Pregnancy or Lack of Contraception Chronic Degenerative Neuromuscular Disease Bladder Cancer or previous record of it Pain of Bladder or Painful Urine Voiding Record of Pelvic Surgery during past one year Excessive Weight Loss Uncontrolled Diabetes

Design outcomes

Primary

MeasureTime frame
Frequency of urinary leakage. Timepoint: At the beginning of the intervention, after 3 and 6 weeks, 1 month after end of intervention. Method of measurement: International Consultation on Incontinence Questionnaire -Urinary Incontinence Short Form (ICIQ-SF) questionnaire.;The amount of urine leakage. Timepoint: At the beginning of the intervention, after 3 and 6 weeks, 1 month after end of intervention. Method of measurement: International Consultation on Incontinence Questionnaire -Urinary Incontinence Short Form (ICIQ-SF) questionnaire.;Time leakage: leakage befor sleep. Timepoint: At the beginning of the intervention, after 3 and 6 weeks, 1 month after end of intervention. Method of measurement: International Consultation on Incontinence Questionnaire -Urinary Incontinence Short Form (ICIQ-SF) questionnaire.;Time of leakage: leakage before reaching the bathroom. Timepoint: At the beginning of the intervention, after 3 and 6 weeks, 1 month after end of intervention. Method of measurement: International Consultation on Incontinence Questionnaire -Urinary Incontinence Short Form (ICIQ-SF) questionnaire.;Time leakage: leakage of urine with coughing and sneezing. Timepoint: At the beginning of the intervention, after 3 and 6 weeks, 1 month after end of intervention. Method of measurement: International Consultation on Incontinence Questionnaire -Urinary Incontinence Short Form (ICIQ-SF) questionnaire.;The leakage of urine: leakage of urine with exercise. Timepoint: At the beginning of the intervention, after 3 and 6 weeks, 1 month after end of intervention. Method of measurement: International Consultation on Incontinence Questionnaire -Urinary Incontinence Short Form (ICIQ-SF) questionnaire.;The leakage of urine: urine leakage after urination immediately prior to wearing underwear. Timepoint: At the beginning of the intervention, after 3 and 6 weeks, 1 month after end of intervention. Method of measurement: International Consultation on Incontinence Questionnaire -Ur

Secondary

MeasureTime frame
Presumptive skin complications. Timepoint: 3 weeks after research start and 6 weeks after that (end of intervention). Method of measurement: Measurement form of drug complications According to Common Terminology Criteria for Adverse Events (CTCAE) Version 5.0.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactLeila Ghanbaryan

Tehran University of Medical Sciences

lghanbaryan@yahoo.com+98 21 8897 4535

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026