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Clinical Trials/CTRI/2014/12/005267
CTRI/2014/12/005267
Completed
未知

Effect of immediate skin-to-skin contact on selected maternal and newborn outcomes after normal delivery

Christian medical college0 sites100 target enrollmentTBD
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ConditionsHealth Condition 1: null- newborn breastfeeding behaviour,thermoregulation, and maternal duration of third stage of labour, blood loss during third and fourth stage of labour and pain perception during perineal wound suturing

Overview

Phase
未知
Intervention
Not specified
Conditions
Health Condition 1: null- newborn breastfeeding behaviour,thermoregulation, and maternal duration of third stage of labour, blood loss during third and fourth stage of labour and pain perception during perineal wound suturing
Sponsor
Christian medical college
Enrollment
100
Status
Completed
Last Updated
4 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
4 years ago
Study Type
Interventional

Investigators

Eligibility Criteria

Inclusion Criteria

  • •1:Primigravida women who do not have any risk factors or may have one or more of the following risk factors\-mild anaemia (Hb of 10\-10\.9 gm%), Rh negative blood group, induction of labour, previous 1 abortion, oligohydramnios which does not require amnioinfusion, polyhydramnios without any anomalies in the fetus, primary infertility, gestational diabetes on diet, obesity, hypothyroidism and short staure primi with height more than 145cm)
  • •2:Women at 36\-42 weeks of gestational age
  • •3:Women between the age group of 19\-32 years
  • •4:Women who come with spontaneous labour
  • •5:Women who deliver normally without the aid of any obstetric instruments
  • •6:Women who deliver with a second degree perineal tear or episiotomy
  • •7:Women who can read English, Tamil or Telugu.
  • •For newborn
  • •1:Newborn with apgar 9 and 10 at 1â?? and 5â?? respectively

Exclusion Criteria

  • •1:High risk primigravida women
  • •2:Women on epidural anaesthesia or entonox
  • •3:Women who develop any third stage complications that warrant emergency/ intensive care
  • •For newborn
  • •1:Newborns with any condition at birth that warrants examination by a neonatologist
  • •2:Newborns with any congenital anomalies which interfere with breastfeeding

Outcomes

Primary Outcomes

Not specified

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