Comparative study on the impact of combined oral contraceptive pills and Progestrogen only pills on the prevalence of bacterial vaginosis using Nugent score : a randomized-controlled trial
Phase 4
- Conditions
- To study prevalence of bacterial vaginosis
- Registration Number
- TCTR20190313002
- Lead Sponsor
- Faculty of Medicine Siriraj Hospital, Mahidol University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending (Not yet recruiting)
- Sex
- Female
- Target Recruitment
- 200
Inclusion Criteria
1. Reproductive age 18-45 years old
2. Women who need oral contraception for 3 months
3. Healthy and no current medication
4. Regular menstrual cycle for 3 consecutive months
5. No history of abnormal vaginal discharge or clinical of vaginitis in 1 month
6. History of postpartum for at least 6weeks and no breastfeeding
Exclusion Criteria
1. History of abnormal uterine bleeding
2. Severe underlying disease
3. History of hormonal contraceptive use within 1 month before enroll in the study
4. Allergic History or contraindication of hormonal contraceptive pill
5. History of prolong antibiotic use or immunosuppressive drug usen
5. Thai women
Pregnant women
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To compare prevalence of bacterial vaginitis on the impact of coc and pop 84 days Nugent score
- Secondary Outcome Measures
Name Time Method To compare the prevalence of STD infection on the impact of COC and POP 84 days Wet smear