Neonatal Outcomes in Instrumental Delivery

Poitiers University Hospital

Status: Completed

Conditions: Instrumental Delivery; Nec, Affecting Fetus or Newborn

Treatments: Other: instrumental delivery

Study type: Observational

Funder types: Other

Identifiers

NCT03337880

CNEI

Details and patient eligibility

About

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.

Enrollment: 300 patients

Sex: All

Ages: 12 to 72 hours old

Volunteers: No Healthy Volunteers

Inclusion criteria

• term infant
• non-opposition of the newborn parent

Exclusion criteria

• outborn child
• premature newborn
• newborn transferred

Trial design

300 participants in 2 patient groups

Cases

Description:

newborns who were delivered with an extractor

Treatment:

Other: instrumental delivery

Controls

Description:

newborns who were not delivered with an extractor