Delayed Umbilical Cord Clamping Amphia Study - ALAAF study
Completed
- Conditions
- Delayed umbilical cord clamping10028920
- Registration Number
- NL-OMON55441
- Lead Sponsor
- Amphia Ziekenhuis
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 100
Inclusion Criteria
- Primary cesarean section
- Duration of pregnance between 37 and 42 weeks
Exclusion Criteria
- Secundary cesarean section
- Maternal clotting disorder
- Maternal irregular antibodies
- Maternal fever
- Prelabor rupture of the membranes (PROM) > 24 hours
- Caesarean section indicated because of placenta praevia
- Caesarean section performed under general anesthesia
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method <p>Outcomes will be divided in primary and secondary outcomes. Main infant study<br /><br>outcomes will be 1) Haemoglobin and haematocrit concentrations 48 hours after<br /><br>birth, 2) APGAR score and 3) Rectal temperature. </p><br>
- Secondary Outcome Measures
Name Time Method <p>Secondary outcomes will be divided into maternal outcomes and outcome of<br /><br>infants.<br /><br><br /><br>Maternal outcomes:<br /><br>1. Maternal blood loss during caesarean section.<br /><br>2. Need for maternal blood transfusion.<br /><br>3. Maternal infections in the postnatal period (6 weeks period)<br /><br><br /><br>Infant outcomes:<br /><br>1. Complete serum bilirubin value 2 days after birth<br /><br>2. Ferritin and Hemoglobin values at the age of 4 months</p><br>