Intrapartum Oxytocin Administration Affects Primitive Neonatal Reflexes
1 other identifier
observational
98
1 country
1
Brief Summary
The aim of this study was to assess whether administration of oxytocin intrapartum (Oxt) has any effect on Neonatal Primitive Reflexes (RNP) and if dose dependent. The secondary objective is to assess the effects on exclusive breastfeeding at 3 months
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
Started Mar 2011
Typical duration for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
March 1, 2011
CompletedPrimary Completion
Last participant's last visit for primary outcome
January 1, 2013
CompletedStudy Completion
Last participant's last visit for all outcomes
June 1, 2013
CompletedFirst Submitted
Initial submission to the registry
June 25, 2013
CompletedFirst Posted
Study publicly available on registry
July 3, 2013
CompletedJuly 3, 2013
June 1, 2013
1.8 years
June 25, 2013
June 27, 2013
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Expression of Neonatal Primitive Reflexes (RNP) are modified by administration of Oxytocin during delivery.
Neonatal Primitive Reflexes studied were: 1) Endogenous: hand to mouth, extension / flexion of fingers, mouth open, tongue extrusion, arm circular motion, circular motion of the leg, flex foot / hand, 2) Antigravity: raise the head, 3) Motors: turn your head, nod, plantar pressure, Babinski, and 4) Rhythmic: suction, jaw movement and swallowing. An observer, blinded to the study group and the dose administered of Oxytocin, valued recordings, analyzing the state of consciousness at the beginning of the recording as Brazelton scale and form RNP dichotomous coding (achieved / not achieved).
72 hours
Secondary Outcomes (1)
Oxytocin intrapartum may have adverse influence on exclusive breastfeeding at 3 months.
6 months
Study Arms (1)
Not exposed to oxytocin
Mother-child dyads in which Oxt had not been administered during the birth process
Interventions
Comparison of Primitive Newborn Reflexes between those exposed or not to Oxytocin
Eligibility Criteria
Maternity ward of a terciary Hospital
You may qualify if:
- Healthy singleton term infant delivered vaginally with Apgar at 5 min\> 7;
- Expressed desire to administer during pregnancy breastfeeding;
- Signed informed consent
You may not qualify if:
- Preterm neonate;
- Fetal chromosomal or other abnormalities diagnosed in utero to modify their adaptation to extrauterine environment;
- Hospitalization of the mother in ICU;
- Hospitalization in the following 48 hours neonate at birth;
- Wish to artificial feeding before parturition;
- Language difficulties;
- Completion of caesarean delivery
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Hospital Universitario Puerta de Hierro-Majadahonda
Madrid, Madrid, 28220, Spain
Related Publications (41)
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PMID: 25785487DERIVED
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Miguel A MarĂn, MD
Hospital Universitario Puerta de Hierro-Majadahonda
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Target Duration
- 6 Months
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- MD Pediatrics-Neonatology
Study Record Dates
First Submitted
June 25, 2013
First Posted
July 3, 2013
Study Start
March 1, 2011
Primary Completion
January 1, 2013
Study Completion
June 1, 2013
Last Updated
July 3, 2013
Record last verified: 2013-06