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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03866876
Other study ID # PHE
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date September 1, 2018
Est. completion date April 2019

Study information

Verified date March 2019
Source Hospices Civils de Lyon
Contact Muriel DORET, Prof.
Phone 4 27 85 51 70
Email muriel.doret-dion@chu-lyon.fr
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Neonatal asphyxia per partum can be complicated by severe neurologic sequelae and can lead to neonatal death. Of the 0.2% of live births to cerebral palsy, 10 to 28% would be secondary to neonatal acidosis. Only metabolic acidosis plays a neurotoxic role, explaining the recent interest of Racinet et al. in the development of a new biochemical marker, more specific than pH or base deficit, of neonatal asphyxia per partum at risk of anoxo-ischemic encephalopathy. This eucapnic neonatal pH raises the hope of a biochemical marker of situations at risk of poor prognosis, with high diagnostic value, prognostic and forensic.

Our hypothesis is that eucapnic pH is more efficient than cord blood arterial pH and base deficit in the prediction of adverse neurologic outcomes.


Recruitment information / eligibility

Status Recruiting
Enrollment 36435
Est. completion date April 2019
Est. primary completion date April 1, 2019
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria:

- All birth more than 37 weeks of amenorrhea at the maternity ward of the hospital Femme-Mère-Enfant

- from 1st of january 2000 to 31 december 2016

Exclusion Criteria:

- Infants born out of the hospital and secondarily hospitalized in the hospital Femme-Mère-Enfant

- Children with congenital anomalies or without valid arterial and venous umbilical cord samples

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Eucapnic pH
Collection of Biological marker (proposed by Racinet): eucapnic pH

Locations

Country Name City State
France Hôpital Femme Mère Enfant Bron

Sponsors (1)

Lead Sponsor Collaborator
Hospices Civils de Lyon

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Number of patients with at least one of these criteria including neonatal seizure, neonatal hypotonia requiring intensive care unit admission, neonatal encephalopathy, and/or neonatal death. Between 2000 and 2016
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