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NCT06227624

Role of Oral Zinc in Reducing Neonatal Indirect Hyperbilirubinemia

Completed Phase 3 Last updated 29 January 2024
What this trial tests

Phase 3 trial testing Oral zinc sulfate and standard phototherapy in Neonatal Jaundice in 192 participants. Completed in 1 January 2020.

Timeline
1 June 2018
Primary endpoint
1 June 2019
1 January 2020

Quick facts

Lead sponsorNational Liver Institute, Egypt
PhasePhase 3
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposetreatment
Enrollment192
Start date1 June 2018
Primary completion1 June 2019
Estimated completion1 January 2020
Sites1 location across Egypt

Drugs / interventions tested

Conditions studied

Sponsor

National Liver Institute, Egypt

Who can join

Adults 1 Hour to 28 Days, any sex, with Neonatal Jaundice. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This study aimed to determine the role of oral zinc in reducing the neonatal indirect hyperbilirubinemia if used concomitant with the standard phototherapy

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other recruiting trials for Neonatal Jaundice

Currently open trials in the same condition.

Other National Liver Institute, Egypt trials

Trials by the same sponsor.

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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/NCT06227624.

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