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Genitourinary Symptoms With Levonorgestrel Releasing Intrauterine Systems

Completed
Conditions
Lower Urinary Tract Symptoms
Registration Number
NCT01730300
Lead Sponsor
Bakirkoy Dr. Sadi Konuk Research and Training Hospital
Brief Summary

The main purpose of the study was to evaluate the efficacy of Levonorgestrel Releasing Intrauterine devices (LNR-IUD) on genitourinary symptoms in patients with abnormal uterine bleeding. The patients were asked urogenital distress inventory (UDI) (which includes; irritative symptoms, stress symptoms, obstructive discomfort) and incontinence impact questionnaire (IIQ) (which includes; physical activity, travel, social/relationships, emotional health)questionnaires in the day of application LNR-IUD and six months later this procedure. Statistical analyse will be performed to evaluate the changes in this time period.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
Female
Target Recruitment
60
Inclusion Criteria
  • women using levonorgestrel releasing intrauterine device for the treatment of menorrhagia or adenomyosis
Exclusion Criteria
  • none

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Urinary frequency6 months

We think that the urinary frequency will be lesser after 6 months of the therapy.

Secondary Outcome Measures
NameTimeMethod
social activity6 months

We think that social activity will be better after reducing urinary symptoms

Trial Locations

Locations (1)

Bakirkoy Dr Sadi Konuk Teaching and Research Hospital, Department of Obstetrics and Gynecology

🇹🇷

Istanbul, Turkey

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