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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT05813730
Other study ID # RIPH 3 / 2022-A02613-40
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date March 2024
Est. completion date December 2024

Study information

Verified date February 2024
Source Central Hospital, Nancy, France
Contact Jean-Michel HASCOET
Phone 0383342934
Email j.hascoet@chru-nancy.fr
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Newborn's renal function is difficult to assess and its physiology during the first days of life is still incompletely known. Studies suggest that the newborn almost completely reabsorbs creatinine during the first 48 to 72 hours of life, while at the same time it continues to produce its own creatinine. Therefore, the initial stock of creatinine at birth still increases through this production and the non or weak clearance. A better knowledge of renal physiopathology in newborns would allow to improve the therapeutic management of the infants, particularly in case of potential nephrotoxicity. No study has attempted to assess the increase in urinary creatinine excretion in neonates from a given time. Objectives: To show when urinary creatinine excretion in newborns is efficient. Results: this study mightr show an inflection point in urinary creatinine excretion illustrating the postnatal age when renal function becomes efficient.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 40
Est. completion date December 2024
Est. primary completion date October 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group N/A to 3 Days
Eligibility Inclusion Criteria: - All full-term newborns (37WA or more) - From a physiological and spontaneous pregnancy - Good neonatal adaptation (Apgar 7 at 5 minutes of life) - Eutrophic (weight > 10th percentile and < 90th percentile) Exclusion Criteria: - Newborns for whom no urine sample is interpretable - Those with a significant clinical-biological anomaly - Neonates with hemodynamic disorders such as low blood pressure (median < gestational age) or hypovolemia (shock, signs of dehydration, need for volume expansion) during the first 3 days of life

Study Design


Related Conditions & MeSH terms


Intervention

Other:
urinary creatinine excretion measurement
Urine samples will be collected up to 6 times a day from birth until discharge from the maternity hospital, to analyze the kinetics of creatinuria.

Locations

Country Name City State
France Maternite Regionale Universitaire CHRU NANCY Nancy Lorraine

Sponsors (1)

Lead Sponsor Collaborator
Central Hospital, Nancy, France

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Longitudinal changes in urinary creatinine excretion in newborns Urine samples will be collected at each diaper change from birth until discharge Longitudinal changes of collected samples from birth until discharge from the maternity hospital (i.e. from birth up to 72 hours postnatal age)
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