Clinical Trials Directory

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.