None listed
Conditions
Interventions
None listed
Sponsors
None listed
Eligibility
Inclusion criteria
Inclusion criteria: 1. Women between 18 to 45 years 2. Willing to choose an intrauterine device (Copper T 380 A or LNG IUS) for contraception. 3. Willing to participate in the study
Exclusion criteria
Exclusion criteria: 1. Pregnancy or suspicion of pregnancy 2. Current or recurrent pelvic inflammatory disease 3. 48 hours - 4 weeks since parturition or abortion 4. Undiagnosed genital tract bleeding 5. Genital tract malformations 6. Known case of genital tract malignancy 7. Known case of breast cancer 8. Adnexal mass 9. History of hydatidiform mole in previous pregnancy 10. Women not willing to participate in the study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| TO ASESS AND COMPARE QUALITY OF LIFE AND SEXUAL FUNCTIONOF COPPER T 380 A VERSUS LNG INTRAUTERINE CONTRACEPTIVE DEVICE USERS USING WHOQOL-BREF QUESTIONNAIRE AND FSFI QUESTIONNAIRE RESPECTIVELYTimepoint: At baseline , at 6 months | — |
Secondary
| Measure | Time frame |
|---|---|
| TO STUDY PAIN DURING INSERTION . TO STUDY AND COMPARE DYSMENORRHEA AND MENSTRUAL BLEEDING PATTERN AT BASELINE ONE MONTH 3 MONTH AND AT 6 MONTHTimepoint: BASELINE ONE MONTH , 3 MONTH AND 6 MONTH | — |
Countries
India
Contacts
AIIMS RISHIKESH