To compare the quality of life and sexual function in two types of intrauterine contraceptive device users
Not Applicable
- Registration Number
- CTRI/2022/05/042813
- Lead Sponsor
- OT APPLICABLE
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 98
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
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
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 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 Outcome Measures
Name Time Method TO STUDY PAIN DURING INSERTION . <br/ ><br>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