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NCT03337880

Neonatal Outcomes in Instrumental Delivery

Completed Last updated 29 January 2019
What this trial tests

trial testing instrumental delivery in Instrumental Delivery; Nec, Affecting Fetus or Newborn in 300 participants. Completed in 4 October 2018.

Timeline
4 December 2017
Primary endpoint
4 October 2018
4 October 2018

Quick facts

Lead sponsorPoitiers University Hospital
StatusCompleted
Study typeOBSERVATIONAL
Enrollment300
Start date4 December 2017
Primary completion4 October 2018
Estimated completion4 October 2018
Sites1 location across France

Drugs / interventions tested

Conditions studied

Sponsor

Poitiers University Hospital

Who can join

Adults 12 Hours to 72 Hours, any sex, with Instrumental Delivery; Nec, Affecting Fetus or Newborn. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other Poitiers University Hospital trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03337880.

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