Trials / Completed
CompletedNCT01730300
Genitourinary Symptoms With Levonorgestrel Releasing Intrauterine Systems
Genitourinary Symptoms in Women Using Levonorgestrel Releasing Intrauterine Systems
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 60 (actual)
- Sponsor
- Bakirkoy Dr. Sadi Konuk Research and Training Hospital · Other Government
- Sex
- Female
- Age
- 15 Years – 55 Years
- Healthy volunteers
- Not accepted
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.
Conditions
Timeline
- Start date
- 2012-06-01
- Primary completion
- 2013-01-01
- Completion
- 2013-05-01
- First posted
- 2012-11-21
- Last updated
- 2013-05-15
Locations
1 site across 1 country: Turkey (Türkiye)
Source: ClinicalTrials.gov record NCT01730300. Inclusion in this directory is not an endorsement.