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临床试验/NCT04663568
NCT04663568终止不适用

Levonorgestrel-releasing Intrauterine System: A Emerging Tool for Conservative Treatment of Pain and Bleeding After Tubal Ligation

Assiut University2 个研究点 分布在 1 个国家目标入组 2 人开始时间: 2020年12月1日最近更新:
适应症

试验速览

阶段
不适用
状态
终止
入组人数
2
试验地点
2
主要终点
The level of pain from before to 6 months after levonorgestrel-releasing intrauterine system insertion

研究概览

简要总结

Today tubal sterilization is a simple, safe, and cost-effective method of achieving long-term contraception. Sterilization is an ideal method of permanent contraception in developing countries where access to health care providers is limited. The percentage of women who use sterilization as a method of contraception rises from about 5% between 20 and 24 years of age to almost 50% for those between 40 and 44 years of age. The most widely touted and most significant health benefit of tubal sterilization appears to be a reduced risk of ovarian cancer.

Post-tubal ligation syndrome includes pain during intercourse, aching lower back, premenstrual tension syndrome, uterine hemorrhage, and absence of menstruation. The syndrome is caused by blood circulation problems in and around the Fallopian tubes and ovaries, pressure on nerves, and intrapelvic adhesion. Since the symptoms of this syndrome are mild, simple symptomatic treatment is sufficient in most cases. In some cases, however, hysterectomy may be necessary.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
30 Years 至 45 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • Women aged from 30-40 year
  • Woman subjected to tubal ligation
  • Women 12 month postpartum
  • Non lactating women
  • Nomedical disorders

排除标准

  • contraindication for Levonorgestrel-releasing Intrauterine System
  • Women with any uterine or ovarian pathology
  • women refuse to participate

结局指标

主要结局

The level of pain from before to 6 months after levonorgestrel-releasing intrauterine system insertion

时间窗: 6 months

visual analogue scale from 0 (minimum value) to 10 (maximum value)

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Mohammed Khairy Ali

Assistant professor

Assiut University

研究点 (2)

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