跳至主要内容
临床试验/CTRI/2024/04/066308
CTRI/2024/04/066308尚未招募1 期

To study the utility of individualized homoeopathic medicine in the pain management of women suffering from Endometriosis

Principal1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2024年5月6日最近更新:

试验速览

阶段
1 期
状态
尚未招募
发起方
入组人数
60
试验地点
1
主要终点
Measure change in severity of pelvic pain as determined by modifications of the VAS score (range 0 to 10) for five modalities of EAPP (dysmenorrhea, deep dyspareunia, non-cyclic pelvic pain, cyclic bowel pain and/or cyclic urinary pain).

研究概览

简要总结

title to study the utility of individualized homoeopathic medicine in pain management in women suffering from Endometriosis. . in the study utility shall be measured using VAS score and SF 36 heath survey. study will start with consent after which detailed homoeopathic case taking will be done on willing patient and medicine shall be given. patient shall be followed up fortnightly. study shall continue for 2 years but min of 6 months follow up shall be required for individual case. Study shall be conducted at NHMC Lucknow

研究设计

研究类型
Interventional
分配方式
Na
盲法
None

入排标准

年龄范围
15.00 Year(s) 至 45.00 Year(s)(—)
性别
Female

入选标准

  • 1 Women of age between 15-45 yrs.
  • 2 Women having symptoms suggesting of endometriosis.
  • 3 Women having USG uterine adnexa shows endometriosis.
  • 4 Women coming to OPD with known case of endometriosis or referred from any other center.

排除标准

  • 1 Women not willing to give their consent for the study.
  • 2 Women having uncontrollable diabetes mellitus, hypertension.
  • 3 Women having life threatening diseases like cancer.

结局指标

主要结局

Measure change in severity of pelvic pain as determined by modifications of the VAS score (range 0 to 10) for five modalities of EAPP (dysmenorrhea, deep dyspareunia, non-cyclic pelvic pain, cyclic bowel pain and/or cyclic urinary pain).

时间窗: At the start of study and every 2 weeks after the start

1 To monitor Ultrasonographical changes

时间窗: At the start of study and every 2 weeks after the start

2 (USG Uterine adnexa) at the end of 6 months of treatment.

时间窗: At the start of study and every 2 weeks after the start

次要结局

  • Measures changes in the scores for quality of life, assessed with SF-36 Health Survey Questionnaire(at start of study then every 2 weeks)

研究者

发起方
Principal
申办方类型
Government medical college
责任方
Principal Investigator
主要研究者

Tripti Gupta

National Homoeopathic Medical College

研究点 (1)

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