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临床试验/CTRI/2018/05/013791
CTRI/2018/05/013791已完成未知

A prospective study of the pattern of drug prescribing for dysfunctional uterine bleeding in a tertiary care hospital

Kempegowda institute of medical sciences and research hospital0 个研究点目标入组 110 人开始时间: 待定最近更新:

试验速览

阶段
未知
状态
已完成
发起方
入组人数
110

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

入选标准

  • 1. Subjects between 20-50 years of age diagnosed as dysfunctional uterine bleeding.
  • 2.Willingness to give written informed consent and availability for regular follow up.

排除标准

  • 1. Subjects with pelvic pathologies such as uterine fibroids, endometriosis, endometrial polyps, PCOS and pelvic inflammatory disease.
  • 2. Pregnant women or lactating women in the first 6 months of postnatal period, women who have had an abortion during the previous 3 months, IUCD or contraceptive pill users.
  • 3. Presence of medical diseases like cardiac dysfunction, uncontrolled diabetes mellitus, uncontrolled hypertension, liver and renal dysfunction, migraine, thyroid disorders, cerebrovascular disease, past or present neoplastic diseases, thromboembolism and coagulation disorders.
  • 4. Women on immunosuppressant therapy, anticoagulation therapy, or who have a known hypersensitivity to any of the drugs used in dysfunctional uterine bleeding.
  • 5. Subjects who have participated in any clinical trial in the past 3 months.

研究者

发起方
Kempegowda institute of medical sciences and research hospital

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