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NCT06227624
Role of Oral Zinc in Reducing Neonatal Indirect Hyperbilirubinemia
Phase 3 trial testing Oral zinc sulfate and standard phototherapy in Neonatal Jaundice in 192 participants. Completed in 1 January 2020.
1 June 2019
Quick facts
| Lead sponsor | National Liver Institute, Egypt |
|---|---|
| Phase | Phase 3 |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | none |
| Primary purpose | treatment |
| Enrollment | 192 |
| Start date | 1 June 2018 |
| Primary completion | 1 June 2019 |
| Estimated completion | 1 January 2020 |
| Sites | 1 location across Egypt |
Drugs / interventions tested
- Oral zinc sulfate and standard phototherapy — full drug profile →
Conditions studied
- Neonatal Jaundice — all drugs for Neonatal Jaundice →
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.
Verify or expand the search:
- PubMed search for NCT06227624
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other recruiting trials for Neonatal Jaundice
Currently open trials in the same condition.
- NCT06963450 — NeoSCB App for Screening Jaundice in Newborns · recruiting
- NCT06399146 — Evaluation of Bilirubin Estimates in Newborns From Smartphone Digital Images in a Population in Botswana · NA · recruiting
- NCT05521607 — Evaluation of a Smartphone-based Screening Tool (Picterus JP) for Neonatal Jaundice (Chicago) · NA · recruiting
Other National Liver Institute, Egypt trials
Trials by the same sponsor.
- NCT07331142 — CBD Stenting vs Non-Stenting for Choledocholithiasis · NA · completed
- NCT06948279 — Immediate vs. Elective Endoscopic Removal of Large CBD Stones in High-Risk Elderly Patients · NA · completed
- NCT07337291 — Double Stent for Biliary Stones in Cirrhotic Patients · NA · completed
- NCT05184491 — Nitazoxanide and Lansoprazole Based Regimens for H. Pylori Management · Phase 4 · unknown
- NCT06384443 — Proton Pump Inhibitors in Cirrhotic Patients · completed
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT06227624 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by National Liver Institute, Egypt
- Last refreshed: 29 January 2024
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