Prenatal Dex Study

Congenital Adrenal Hyperplasia Clinical Trial

— Prenatal Dex  

Official title:

Multicentric Evaluation of in Utero Dexamethasone (DEX) on the Cognitive Development of Children at Risk of Congenital Adrenal Hyperplasia

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT02795871
• Other study ID #: 69HCL14_0447
• Status: Recruiting
• Phase: N/A
• First received: May 25, 2016
• Last updated: February 21, 2017
• Start date: October 2016
• Est. completion date: December 2019

Study information

• Verified date: February 2017
• Source: Hospices Civils de Lyon
• Contact: Véronique TARDY-GUIDOLLET, MD PHD
• Phone: (0)4.72.12.96.35
• Email: veronique.tardy[@]chu-lyon.fr
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The classic form of 21-hydroxylase deficiency (prevalence 1/15,000) is the most common cause of congenital adrenal hyperplasia (CAH). This autosomic recessive disease is responsible for virilization of the external genitalia in girls through androgen hypersecretion during fetal life. Since 1984, the Lyon Pediatric Endocrinology group has proposed prenatal dexamethasone (DEX) for all fetuses at risk of CAH With the aim of preventing fetal androgen hypersecretion in affected girls and avoiding poor long-term results from reconstructive surgery. Prenatal DEX was used in Europe and the USA but its use was recently suspended: in 2007, a Swedish study conducted on 26 children treated with DEX in utero for a short period of time reported cognitive impairments. These data were not confirmed by an American study on the short-term DEX use, which showed potential cognitive impairments in CAH children exposed to DEX for long periods of time. These confusing and controversial results have caused the scientific community to question its position and have resulted in the suspension of the use of prenatal DEX with drastic consequences for CAH girls (virilization; genital surgery etc.). In this context, an evaluation of neuropsychological development under in utero DEX is essential to validate its indication for use during the prenatal period. This study will evaluate outcomes using prospective cognitive and emotional assessments. It will first focus on the unaffected children previously treated in utero in order to assess the adverse effects of the drug. The study will then assess the children with CAH for whom DEX could have beneficial effects.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 500
• Est. completion date: December 2019
• Est. primary completion date: December 2018
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 6 Years to 15 Years

Eligibility

Inclusion Criteria:

Groups D+1, D+2, D-1 and D-2

• Male or female

• Patient with Congenital Adrenal Hyperplasia or sibling of a CAH patient

• Age: 6 to 15 years (at the time of inclusion)

• The subject's legal representatives have understood the information note/informed consent form, obtained answers to all their questions and have given signed, written, informed consent

• Subject with health insurance

Group D-3 (Schoolchildren)

• Male or female

• With no connection with Congenital Adrenal Hyperplasia

• Age: 6 to 15 years (at the time of inclusion)

• The subject's legal representatives have understood the information note/informed consent form, obtained answers to all their questions and have given signed, written, informed consent

• Subject with health insurance

Exclusion Criteria:

For all groups :

• Patient/Subject with another genetic disease

• Patient/Subject with known neuropsychology disease(s)

• Patient/Subject whose mother has received another treatment during her pregnancy with possible known adverse events on the neuropsychological development of the child

Related Conditions & MeSH terms

• Adrenal Hyperplasia, Congenital
• Adrenocortical Hyperfunction
• Adrenogenital Syndrome
• Congenital Adrenal Hyperplasia
• Hyperplasia

Intervention

Behavioral:
• Neuropsychological and cognitive assessment

Locations

Country	Name	City	State
France	Groupement Hospitalier Est - Laboratoire d'endocrinologie moléculaire et maladies rares - Centre de biologie et de pathologie Est. 59 boulevard Pinel	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	Intelligence quotient	Wechsler Intelligence Scale for Children (WISC) is designed to measure human intelligence. WISC-IV includes: Verbal Comprehension Index: measure of verbal concept formation.; Perceptual Reasoning Index: measure of non-verbal and fluid reasoning.; Working Memory Index: measure of working memory.; Processing Speed Index: measure of processing speed. Data measured: raw score (0 to 150), standard score (1 to 19), index (40 to 160).; The four indexes of the intelligence quotient will be considered hierarchically as follows: first the Working Memory Index, then the Processing Speed Index, third the Perceptual Reasoning Index, fourth the Verbal Comprehension Index.	3 months
Secondary	Children Memory Scale (CMS)	Neurocognitive profile of children assessed by Children Memory Scale (CMS) at Visit 2.; Memory tests: Children Memory Scale (CMS), the following composites will be considered in our study: Immediate and delayed visual memory : face recognition and dot location; Immediate and delayed verbal memory, recognition : stories, word pairs; Learning: dot location and word pairs; Attention, concentration: numbers, sequences	3 months
Secondary	Rey figure test	Neurocognitive profile of children assessed by visuoperceptual test (Rey Figure test) at Visit 2	3 months
Secondary	Revised - Child Measure of Anxiety Scale (R- CMAS) score	Emotional profile assessed by Revised - Child Measure of Anxiety Scale (R- CMAS) score	15 months
Secondary	Mood Depressive Inventory for Children (MDI- C) score	Emotional profile assessed by Mood Depressive Inventory for Children (MDI- C) score	15 months
Secondary	Child Behavior Checklist (CBCL) score	Emotional profile assessed by Child Behavior Checklist (CBCL) score	15 months
Secondary	Evaluation of the benefits of in utero DEX in preventing or reducing the virilization of external genitalia in CAH girls	The anatomical evaluation (phenotyping) of girls' external genitalia was performed at the time of the surgical correction and included the measurement of the genital tubercule (GT), the distance between the perineum and the urethra-vaginal confluence, the degree of fusion of the genital folds (labia majora), their pigmentation and creases. The measurement of the ano-genital distance was not routine practice in the past.	Day 1