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临床试验/NCT01730300
NCT01730300已完成不适用

Genitourinary Symptoms in Women Using Levonorgestrel Releasing Intrauterine Systems

Bakirkoy Dr. Sadi Konuk Research and Training Hospital1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2012年6月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
60
试验地点
1
主要终点
Urinary frequency

研究概览

简要总结

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.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
15 Years 至 55 Years(Child, Adult)
性别
Female
接受健康志愿者

入选标准

  • women using levonorgestrel releasing intrauterine device for the treatment of menorrhagia or adenomyosis

排除标准

  • 未提供

结局指标

主要结局

Urinary frequency

时间窗: 6 months

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

次要结局

  • social activity(6 months)

研究者

发起方
Bakirkoy Dr. Sadi Konuk Research and Training Hospital
申办方类型
Other Gov
责任方
Principal Investigator
主要研究者

murat ekin

Training Officer of Obstetrics and Gynecology Department M.D.

Bakirkoy Dr. Sadi Konuk Research and Training Hospital

研究点 (1)

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