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Clinical Trial 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.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms

  • Instrumental Delivery; Nec, Affecting Fetus or Newborn

NCT number NCT03337880
Study type Observational
Source Poitiers University Hospital
Contact
Status Completed
Phase
Start date December 4, 2017
Completion date October 4, 2018