A comparison between the side effects of two methods of Contraceptio
Phase 2
- Conditions
- Contraception.General counselling and advice on contraception
- Registration Number
- IRCT138903242624N6
- Lead Sponsor
- Iran University of Medical Sciences, Deputy of Research and Technology
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 1000
Inclusion Criteria
non pregnant and married women who are 18-35 years old and are serious for not to be pregnant during the next year and their BMI is in the normal range (19-25). Exclusion criteria: history of breast cancer, endometrial cancer, abnormal uterine bleeding , being smoker, active or chronic liver disease , obstructive jaundice, liver adenoma or carcinoma, liver cirrhosis, thromboembolic disorders, heart disease, stroke, diabetes, hypertension, recurrent headache or dizziness, history of depression or anxiety, breast feeding, dislipidemia, any systemic disorder or any drug use for systemic disorders, AUB , Oligomenorhea.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Adverse effects. Timepoint: 1-3-6-12 months. Method of measurement: questionnaire.
- Secondary Outcome Measures
Name Time Method The frequency of discontinuation of contraception. Timepoint: 1-3-6-12 months. Method of measurement: Questionnaire.