Health Condition 1: N800- Endometriosis of uterus
Conditions
Interventions
Intervention1: Levonorgestrel intrauterine device: One group of people with endometriosis related chronic pelvic pain will be given levonorgestrel releasing intrauterine device .It will be inserted in
Sponsors
Riddhi Pushilal
Eligibility
Inclusion criteria
Inclusion criteria: 1. Patients having confirmed diagnosis of endometriosis 2.Women with diagnosis of deep endometriosis by TVUS or MRI 3.Those who are on other management for endometriosis will be included after washout period
Exclusion criteria
Exclusion criteria: 1.Women who cannot use either of the two hormonal implants as prescribed by WHO 2.Women who have undergone surgical intervention for symptom management with 2months of enrolment in the study. 3.Women who wish to conceive within the next 12 months. 4.Women who are not otherwise healthy 5.Women who are not willing to keep a menstrual diary to record their bleeding and pain levels 6.Age of the patient is not within 18-45 years 7.If the patient is not willing to follow up in the Out Patient s Department 8.The patient s unwilling to adopt either of the proposed treatment alternative
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Primary outcome : The primary outcome measures the improvement in the level of pain felt during each cycle of menstruation after the insertion of the implant as compared to the month before. Timepoint: The primary outcome will be measured as improvement in pain levels after 90 days | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary outcome : The secondary outcome will be the improvement in the quality of life & noncyclic pain after the intervention as compared to before. Timepoint: The secondary outcome will be studied in a span of 90 days | — |
Countries
India
Contacts
Public ContactRiddhi Pushilal
Ipgmer
Outcome results
None listed