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NCT04087148

Linear Growth of Children With Congenital Adrenal Hyperplasia

Status unknown Last updated 12 September 2019
What this trial tests

trial in Congenital Adrenal Hyperplasia in 60 participants. Status unknown.

Timeline
24 September 2019
Primary endpoint
24 October 2020
24 October 2021

Quick facts

Lead sponsorAssiut University
StatusStatus unknown
Study typeOBSERVATIONAL
Enrollment60
Start date24 September 2019
Primary completion24 October 2020
Estimated completion24 October 2021

Conditions studied

Sponsor

Assiut University

Who can join

Adults 1 to 18, any sex, with Congenital Adrenal Hyperplasia. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The congenital adrenal hyperplasias (CAHs) comprise a family of autosomal recessive disorders that disrupt adrenal steroidogenesis. Three specific enzyme deficiencies are associated with virilization of affected women. The most common form is 21-hydroxylase deficiency (21-OHD) due to mutations in the 21-hydroxylase (CYP21A2) gene. Other virilizing forms include 3b-hydroxysteroid dehydrogenase type 2 (HSD3B2) and 11b-hydroxylase deficiencies associated with mutations in the HSD3B2 and 11b-hydroxylase (CYP11B1) genes, respectively.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Congenital Adrenal Hyperplasia

Currently open trials in the same condition.

Other Assiut University trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04087148.

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