A clinical trial to study the effect of different timings of clamping the umbilical cord on the general health of the newborn baby.
Not Applicable
- Conditions
- Health Condition 1: O80- Encounter for full-term uncomplicated delivery
- Registration Number
- CTRI/2019/03/018259
- Lead Sponsor
- Armed Forces
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Singleton pregnancy more than 36 weeks of gestation.
Uncomplicated vaginal delivery
Exclusion Criteria
unwilling to participate
instrumental delivery
haemodyanamic instability
antepartum haemmorrhage
IUGR in foetus detected by usg
need for immediate resuscitation in new born
tight nucal cord in newborn warranting immediate clamping and cutting of cord
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method