Pain management in endometriosis by Homoeopathic medicine
Phase 1
- Conditions
- Health Condition 1: N809- Endometriosis, unspecified
- Registration Number
- CTRI/2024/04/066308
- Lead Sponsor
- Principal
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1Women of age between 15-45 yrs.
2Women having symptoms suggesting of endometriosis.
3Women having USG uterine adnexa shows endometriosis.
4Women coming to OPD with known case of endometriosis or referred from any other center.
5Women who are willing to participate in the study.
Exclusion Criteria
1Women not willing to give their consent for the study.
2Women having uncontrollable diabetes mellitus, hypertension.
3Women having life threatening diseases like cancer.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 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). <br/ ><br>1To monitor Ultrasonographical changes <br/ ><br>2(USG Uterine adnexa) at the end of 6 months of treatment. <br/ ><br>Timepoint: At the start of study and every 2 weeks after the start <br/ ><br>
- Secondary Outcome Measures
Name Time Method Measures changes in the scores for quality of life, assessed with SF-36 Health Survey QuestionnaireTimepoint: at start of study then every 2 weeks