Management of Cervical Erosion in Ayurveda
- Conditions
- Health Condition 1: null- cervical erosionHealth Condition 2: N86- Erosion and ectropion of cervix uteri
- Registration Number
- CTRI/2018/01/011329
- Lead Sponsor
- Institute fot Post Graduate Teaching and Research in Ayurveda
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 30
2.Patients with clinical signs and symptoms including white discharge/abnormal vaginal discharge, contact bleeding, backache, O/E presence of cervical erosion with cervicitis/ endocervicitis/ hypertrophy, unhealthy cervix, Nabothian cyst etc. or only presence of cervical erosion will be included in the study
Pap smear confirming chronic cervicitis or CIN I(As per Bethesda classification)
Yogya for Agnikarma
Unmarried women will be excluded
Women below 21 years and above 60 years
3Pregnant women and lactating mothers
Patients suffering with following condition will be excluded from study
Tuberculosis of uterus and endometrium
Cervical polyp
Procedentia
CIN Grade II and III (As per Bethesda classification)
Other chronic debilitating disorders such as TB uncontrolled DM etc
Ayogya for Agnikarma
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Improvement in signs and symptoms of the disease <br/ ><br>Improvement in general health condition of the patients <br/ ><br> <br/ ><br>Suitable scoring pattern shall be developed The gradation system will be adopted for the site and size appearance type and degree of eroded area <br/ ><br>Objective Criteria <br/ ><br>Changes in Pap smear report BT and AT <br/ ><br>Improvement in other investigatory parametersTimepoint: 1 month
- Secondary Outcome Measures
Name Time Method Improvement in signs and symptoms of the disease <br/ ><br>Improvement in general health condition of the patients <br/ ><br> <br/ ><br>Suitable scoring pattern shall be developed The gradation system will be adopted for the site and size appearance type and degree of eroded area <br/ ><br>Objective Criteria <br/ ><br>Changes in Pap smear report BT and AT <br/ ><br>Improvement in other investigatory parameters <br/ ><br>Timepoint: 1 month
Related Research Topics
Explore scientific publications, clinical data analysis, treatment approaches, and expert-compiled information related to the mechanisms and outcomes of this trial. Click any topic for comprehensive research insights.