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To study the effects of 2 standard treatment-timing strategies for glucocorticoïd dosage on androgen concentration in CAH children

Optimizing timing of glucocorticoid treatment in children with congenital adrenal hyperplasia

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON25245
Enrollment
50
Registered
2020-08-12
Start date
2019-06-13
Completion date
Unknown
Last updated
2024-02-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Congenital adrenal hyperplasia (AGS)

Interventions

After the informed consent procedure, each patient will recieve the same total daily medication dosage from their own initial pre-study treatment, starting with either the biggest dosage of hydrocorti

Sponsors

Radboudumc, Department of pediatric endocrinology
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: • Children and adolescents with CAH due to 21-hydroxylase deficiency > 4 years old • The diagnosis is confirmed by mutation analysis • Patient are treated with hydrocortisone according to standard guidelines in a thrice daily schedule • Ability to collect saliva

Exclusion criteria

Exclusion criteria: • Other forms of CAH • Not able to collect saliva • Chronical medication use other than hydrocortisone and fludrocortisone

Design outcomes

Primary

MeasureTime frame
Concentrations of salivary 17OHP and A after 3 weeks of treatment with the 2 different timing strategies.

Secondary

MeasureTime frame
12 Hours blood pressure and activity and sleeping patters during the 2 treatment strategies.

Contacts

Public ContactHedi Claahsen - van der Grinten, MD PhD

Radboudumc

Hedi.claahsen@radboudumc.nl+31 24 36 14 430

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)