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NCT05977972

Pattern of Metabolic Causes of Neonatal Hypoglycemia

Status unknown Last updated 7 August 2023
What this trial tests

trial in Neonatal Hypoglycemia in 100 participants. Status unknown.

Timeline
1 October 2023
Primary endpoint
1 June 2024
1 August 2024

Quick facts

Lead sponsorAssiut University
StatusStatus unknown
Study typeOBSERVATIONAL
Enrollment100
Start date1 October 2023
Primary completion1 June 2024
Estimated completion1 August 2024

Conditions studied

Sponsor

Assiut University

Who can join

Adults 1 Day to 28 Days, any sex, with Neonatal Hypoglycemia or Metabolic Disease. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Inborn errors of metabolism (IEM) are disorders in which there is a block at some point in the normal metabolic pathway caused by a genetic defect of a specific enzyme. The number of diseases in humans known to be attributable to inherited point defects in metabolism now exceeds 500.While the diseases individually are rare, they collectively account for a significant proportion of neonatal and childhood morbidity and mortality. Diagnosis is important not only for treatment and prognostication but also for genetic counselling and antenatal diagnosis in subsequent pregnancies.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Neonatal Hypoglycemia

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/NCT05977972.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing