Aldosterone Resistance in Preterm Infants (PREMALDO)

This study is ongoing, but not recruiting participants.
Sponsor:
Collaborator:
Institut National de la Santé Et de la Recherche Médicale, France
Information provided by (Responsible Party):
Assistance Publique - Hôpitaux de Paris
ClinicalTrials.gov Identifier:
NCT01176162
First received: July 6, 2010
Last updated: April 3, 2013
Last verified: April 2013

July 6, 2010
April 3, 2013
January 2010
June 2013   (final data collection date for primary outcome measure)
urinary aldosterone [ Time Frame: during the first year of life ] [ Designated as safety issue: No ]
Determination of normal values of urinary aldosterone concentration in each group (24 first hours, day three, and at 1 and 3 months)
urinary aldosterone [ Time Frame: during the first year of life ] [ Designated as safety issue: No ]
Determination of normal values of urinary aldosterone concentration in each group (24 first hours, day three, and at 1,3, 6 and 12 months)
Complete list of historical versions of study NCT01176162 on ClinicalTrials.gov Archive Site
  • plasma electrolytes concentrations [ Time Frame: first year of life ] [ Designated as safety issue: No ]
    Comparison of plasma and urinary electrolytes concentrations with hormonal measurements and clinical parameters. Evolution of these biological parameters throughout the first year of life, depending on gestational age at birth.
  • urinary electrolytes concentrations [ Time Frame: first year of life ] [ Designated as safety issue: No ]
    Comparison of plasma and urinary electrolytes concentrations with hormonal measurements and clinical parameters. Evolution of these biological parameters throughout the first year of life, depending on gestational age at birth.
  • hormonal measurements [ Time Frame: first year of life ] [ Designated as safety issue: No ]
    Comparison of plasma and urinary electrolytes concentrations with hormonal measurements and clinical parameters. Evolution of these biological parameters throughout the first year of life, depending on gestational age at birth.
  • clinical parameters [ Time Frame: first year of life ] [ Designated as safety issue: No ]
    Comparison of plasma and urinary electrolytes concentrations with hormonal measurements and clinical parameters. Evolution of these biological parameters throughout the first year of life, depending on gestational age at birth.
Same as current
Not Provided
Not Provided
 
Aldosterone Resistance in Preterm Infants
PREMALDO : Aldosterone Resistance in Preterm Infants : Assessment by a Non Invasive Measurement of Urinary Aldosterone

In the neonatal period, the human kidney is characterized by a functional immaturity responsible for an impaired ability to regulate water and sodium homeostasis, which is exacerbated by prematurity. This altered sodium handling could be related to a partial renal aldosterone resistance. Renal sodium reabsorption and potassium excretion are mainly controlled by aldosterone, after binding to the mineralocorticoid receptor (MR). The investigators have analyzed MR expression throughout human and mouse renal development, and the investigators found a weak MR expression at birth. The investigators have conducted a pilot study in full-term newborns, which confirmed a partial neonatal aldosterone resistance. This study also highlighted that urinary aldosterone is the best index to accurately assess aldosterone sensitivity at birth.

Principal objective:

To assess aldosterone resistance at birth by a non invasive measurement of urinary aldosterone, in order to evaluate its intensity as a function of gestational age. Determination of normal values of urinary aldosterone concentration in each group.

Secondary objectives:

Comparison of plasma and urinary electrolytes concentrations with hormonal measurements and clinical parameters. Evolution of these biological parameters throughout the first year of life, depending on gestational age at birth.

Methodology : multicentric study, open study Two hundred-forty newborns will be included in order to constitute 4 groups of 60 children, classified according to their gestational age: < 28 GW, 28 - < 33 GW, 33- < 37 GW, > 37 GW.

Inclusion criteria: every newborn will be included, after written parental consent was obtained.

Study :

Urinary samples will be collected onto a gauze compress, during the first 24 hours of life, at day three, and at 1, 3, 6 and 12 months. A blood sample will be obtained from systematic umbilical cord blood collection at birth and during the Guthrie test at day three. Aldosterone and renin concentrations will be measured in BICETRE Hospital laboratory. Plasma and urinary electrolyte concentrations will be measured in the Biochemistry department. DNA samples will also be gathered from umbilical cord blood for future genetic investigations (functional polymorphisms of the MR gene).

Perspectives This study will permit to assess the intensity of aldosterone resistance in full-term and preterm newborns, by a non invasive method. It should bring new insights into the mechanisms of hormonal regulation of sodium balance in preterm newborns and during the first year of life. Urinary aldosterone assessments may open new perspectives for therapeutic management of water and sodium waste in premature infants.

Observational
Observational Model: Case-Only
Time Perspective: Prospective
Not Provided
Retention:   Samples Without DNA
Description:
  • Urinary samples will be collected onto a gauze compress, during the first 24 hours of life, at day three, and at 1, 3, 6 and 12 months.
  • A blood sample will be obtained from systematic umbilical cord blood collection at birth and during the Guthrie test at day three
Non-Probability Sample

Every newborn without congenital malformation will be included, after written parental consent was obtained

Newborn
Not Provided
  • Group "< 28"
    • Gestational Age < 28 weeks
  • Group "28 - < 33"
    • Gestational Age : 28 - < 33 weeks
  • Group "33- < 37"
    Gestational Age : 33- < 37 weeks
  • Group "> 37"
    Gestational Age > 37 weeks
Martinerie L, Viengchareun S, Delezoide AL, Jaubert F, Sinico M, Prevot S, Boileau P, Meduri G, Lombès M. Low renal mineralocorticoid receptor expression at birth contributes to partial aldosterone resistance in neonates. Endocrinology. 2009 Sep;150(9):4414-24. Epub 2009 May 28.

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Active, not recruiting
170
December 2013
June 2013   (final data collection date for primary outcome measure)

Inclusion criteria :

  • Maternal

    • Maternal age ≥ 18 and ≤ 45 years,
    • Written parental consent
    • Normal obstetrical ultrasounds
  • Neonatal - Birth by vaginal delivery or cesarean section

Exclusion criteria :

  • Maternal

    • Type 1 or type 2 diabetes,
    • Adrenal or hypophyseal deficiency
    • Treatment for arterial hypertension
  • Neonatal

    • Perinatal anoxia (defined by an Apgar score < 5 at 5 min and pH < 7,10 and lactacidemia > 9 mmol/l at blood cord).
    • Congenital malformation
    • Chromosomic abnormalities
Both
24 Weeks to 41 Weeks
No
Contact information is only displayed when the study is recruiting subjects
France
 
NCT01176162
P081211, B91017-20
No
Assistance Publique - Hôpitaux de Paris
Assistance Publique - Hôpitaux de Paris
Institut National de la Santé Et de la Recherche Médicale, France
Principal Investigator: Pascal BOILEAU, MD PhD Assistance Publique - Hôpitaux de Paris
Assistance Publique - Hôpitaux de Paris
April 2013

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP