EFFICACY OF TRANEXAMIC ACID IN REDUCING POSTPARTUM BLOOD LOSS FOLLOWING VAGINAL DELIVERY: A DOUBLE-BLIND PLACEBO CONTROLLED RANDOMIZED CLINICAL STUDY IN NAUTH, NNEWI
Not Applicable
- Conditions
- Postpartum blood loss
- Registration Number
- PACTR202211791554683
- Lead Sponsor
- naedozie Paul Obiegbu
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- Female
- Target Recruitment
- 110
Inclusion Criteria
1. 18years and above at time of consent
2. Singleton pregnancy
3. Term gestation ( = 37 completed weeks)
Exclusion Criteria
1. Multiple pregnancy
2. History of eclampsia or pre-eclampsia in index pregnancy
3. Imminent delivery (<2 hours) from presentation
4. History of bleeding disorders
5. History of allergy to tranexamic acid
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method