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NCT03337880
Neonatal Outcomes in Instrumental Delivery
trial testing instrumental delivery in Instrumental Delivery; Nec, Affecting Fetus or Newborn in 300 participants. Completed in 4 October 2018.
4 October 2018
Quick facts
| Lead sponsor | Poitiers University Hospital |
|---|---|
| Status | Completed |
| Study type | OBSERVATIONAL |
| Enrollment | 300 |
| Start date | 4 December 2017 |
| Primary completion | 4 October 2018 |
| Estimated completion | 4 October 2018 |
| Sites | 1 location across France |
Drugs / interventions tested
- instrumental delivery
Conditions studied
- Instrumental Delivery; Nec, Affecting Fetus or Newborn — all drugs for Instrumental Delivery; Nec, Affecting Fetus or Newborn →
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.
Verify or expand the search:
- PubMed search for NCT03337880
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
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Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT03337880 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Poitiers University Hospital
- Last refreshed: 29 January 2019
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.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing