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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT06391476
Other study ID # CRC_GHN_2024_001
Secondary ID
Status Completed
Phase
First received
Last updated
Start date January 1, 2021
Est. completion date December 31, 2022

Study information

Verified date April 2024
Source Hospices Civils de Lyon
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Advancements in perinatal care have significantly improved the survival of extremely premature infants, establishing a viability threshold below 25 weeks' gestational age (GA). However, management at the limit of viability poses ethical and decision-making problems for health-care professionals. They grapple with the delicate balance between potential survival and long-term disabilities. These decisions, as well as the information given to families, are based on knowledge of the prognosis as assessed by national and international epidemiological studies. Healthcare professionals rely on population-based estimations but face discrepancies in predicting outcomes because there are significant variation depending on perinatal center and country where infants are hospitalized. In the large French epidemiological study, 9,6% of livebirths included were born at 22-25 wks and only 38% survived. In the neonatology department of the croix rousse, these infants have been actively cared for for many years, which has allowed the development of specific skills that are essential for the proper management of these very high-risk patients. Furthermore, EPIPAGE 2 included data from centers where perinatal management was probably not very active at these extreme ages. It results in worse neonatal outcomes as evaluated at the national level than outcomes data evaluated at the neonatal intensive care unit of Croix-Rousse hospital. Using data from EPIPAGE 2 study for clinical decision could lead to avoid active care at the for some infants at the limit of viability It is needed to obtain complete evaluation of neonatal outcomes of infants hospitalized at the Croix-Rousse hospital, so that clinicians may rely on actualized data related to the practices in their perinatal center. It is also needed to compare outcomes with data from large national and international cohorts, to identify and quantify differences. Data about later neurodevelopment outcomes, at 2 years, are also needed as it can taken in consideration in decision-making process.


Recruitment information / eligibility

Status Completed
Enrollment 300
Est. completion date December 31, 2022
Est. primary completion date September 30, 2022
Accepts healthy volunteers No
Gender All
Age group 22 Weeks to 25 Weeks
Eligibility Inclusion Criteria: - Infants born between 22 and 25 weeks gestational age - Infants hospitalized at the tertiary care neonatal unit of Croix-Rousse hospital - Infants born between January 2010 and December 2019 Exclusion Criteria: - None

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Study of the evolution of a cohort of children born between 22 and 25 weeks gestational age
Study of mortality in a cohort of children born between 22 and 25 weeks gestational age Study of neonatal morbidity Description of postnatal growth Description of nutrition and breastfeeding at discharge Study of the neurological, respiratory and growth outcome at 2 years.

Locations

Country Name City State
France Hôpital Croix Rousse Lyon Rhone

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 Mortality Proportion of deaths in a cohort of infants born between 22 - 25 weeks gestational age up to 24 months corrected age
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