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Neonatal Outcomes in Instrumental Delivery

NCT03337880 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 300

Last updated 2019-01-29

No results posted yet for this study

Summary

The aim of this study is to compare the impact of instrumental delivery on newborn head mark and newborn comfort over the impact of non-instrumental delivery. It is also to evaluate how mothers age, Body Mass Index, instrumental extraction indication, extractor type, variety and height of the fetal presentation, operator, time of birth (day or night) and birth weight impact on head mark existence and newborn comfort.

Conditions

  • Instrumental Delivery; Nec, Affecting Fetus or Newborn

Interventions

OTHER

instrumental delivery

the birth was assisted with an extractor.

Sponsors & Collaborators

  • Poitiers University Hospital

    lead OTHER

Eligibility

Min Age
12 Hours
Max Age
72 Hours
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-12-04
Primary Completion
2018-10-04
Completion
2018-10-04

Countries

  • France

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03337880 on ClinicalTrials.gov