A clinical trial to study of Brihtyadi Ghan vati and laghu panchmoola kwath prakshalan and taila pichu in paripluta yonivyapad wsr PID
Phase 1
- Conditions
- Health Condition 1: N739- Female pelvic inflammatory disease, unspecified
- Registration Number
- CTRI/2023/08/056761
- Lead Sponsor
- State Ayurvedic college and hospital Lucknow UP
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1• Patient willing for trial.
2• Married women
3• lower abdomen pain
4• Low back pain.
5• Abnormal cervical or vaginal discharge
6• Dyspareunia
Exclusion Criteria
1• Pregnant women
2• Unmarried
3• PID associated with prolapsed uterus.
4• Endometriosis/ Chocolate cyst.
5• Severe or chronic ill health condition like diabetes mellitus & Hypertension tuberculosis
etc.
6• Acute PID & peritonitis, tubo- Ovarian abscess, Genital tumor & malignancy.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1)To assess the efficacy of Brihatyadi Ghan vati and Laghu Panchmula kwath prakshalan <br/ ><br>with taila pichu in management of Paripluta Yonivyapad <br/ ><br> <br/ ><br>2)To assess the efficacy of trial therapy on <br/ ><br>subjective parameters like pain in lower abdomen low back pain vaginal discharge dyspareunia objective criteria like cervical motion tenderness fornix tendernessTimepoint: Final assessment will be done after completion <br/ ><br>of trial of 4 consecutive months (3 months with <br/ ><br>clinical therapy and 1 month drug free)
- Secondary Outcome Measures
Name Time Method To assess the efficacy of trial therapy on <br/ ><br>subjective parameters like pain in lower abdomen low back pain vaginal discharge dyspareunia objective criteria like cervical motion tenderness fornix tenderness USG finding ( fluid in pouch of Douglas)Timepoint: Follow up- Three follow up will be done at every 1month during the therapy