A clinical trial to study the effect of clindamycin in patients with vaginal pH MORE THAN OR EQUAL TO 5 to prevent pretermlabour
Phase 2
Completed
- Conditions
- Health Condition 1: null- pregnancyHealth Condition 2: O600- Preterm labor without delivery
- Registration Number
- CTRI/2011/10/002045
- Lead Sponsor
- Pallavi chalasani
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 210
Inclusion Criteria
Pregnant women 13 to 16 plus minus 1 week period of gestation.
Singleton pregnancy
vaginal pH more than or equal to 5
Exclusion Criteria
Not willing to provide informed concent
History of antibiotic use with in the previous 14 days
Current placement of cervical cerclage
Current recepit of tocolytic therapy
History of cone biopsy
Significant known medical complications diabetes, renal disease, collagen disease, epilepsy, lupus, antiphospholipid syndrome, essential hypertention
Uterine or cervical anomaly
Life threatening known fetal anomaly
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method preterm labourTimepoint: preterm labour
- Secondary Outcome Measures
Name Time Method low birth weight , misscarriagesTimepoint: low birth weight , misscarriages