Health Condition 1: N945- Secondary dysmenorrhea
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Women aged 20 to 45 years with regular menstrual cycles (28 7 days), diagnosed with congestive dysmenorrhea, and willing to participate in the study will be included. Participants should have a clinical and/or ultrasonographic diagnosis of congestive dysmenorrhea associated with one or more underlying pelvic pathologies, namely endometriosis, adenomyosis, uterine fibroids, chronic pelvic inflammatory disease, acquired retroversion of the uterus, or endometrial polyp. Only those fulfilling the above criteria will be enrolled in the study.
Exclusion criteria
Exclusion criteria: Women with endometriotic cysts larger than five centimetres, malignancy, intrauterine contraceptive device in situ, elevated serum CA 125 levels above thirty five units per millilitre, pregnancy or lactation, or uncontrolled systemic illness will be excluded.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Menstrual pain intensity Assessed using the Visual Analogue Scale (VAS).Timepoint: At baseline,4th week,8th week and 12th week(follow-up) | — |
Secondary
| Measure | Time frame |
|---|---|
| Vaginal pH using standard pH stripsTimepoint: At baseline,8th week (after treatment period),12th week (followup) | — |
Countries
India
Contacts
Government Ayurveda College , Tripunithura