Maternal and neonatal effects of different umbilical cord clamping method after delivery in Ilorin: A randomised control study.
Not Applicable
Recruiting
- Conditions
- Pregnancy and Childbirthmaternal blood losss after delivery to rule out postpartum haemorrhagePaediatrics
- Registration Number
- PACTR202404884596632
- Lead Sponsor
- AKERAADEGBOYEGA GANIYAT
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 168
Inclusion Criteria
•A pregnant woman who consented herself and her baby to participate in the study.
•Intrapartum haemoglobin concentration =10g/dl
•Spontaneous vaginal delivery
•A live vigorous baby at birth.
Exclusion Criteria
•Umbilical cord abnormalities e.g true knots, pseudoknots.
•Rhesus negative women
•Patient with chronic medical conditions e.g Sickle cell disease, diabetes mellitus.
•Maternal infections e.g patient with hepatitis B, hepatitis C and HIV
•Antenatally diagnosed congenital anomaly or apparent at birth.
•Antepartum haemorrhage
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method