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NCT05134792

Effect of Pre-emptive Intravenous Immunoglobulin (IVIG) on the Incidence of Septic Episodes in Pediatric Burn Patients

Completed Phase 2, PHASE3 Last updated 15 November 2022
What this trial tests

Phase 2, PHASE3 trial testing intravenous immunoglobulin in Burn Shock in 30 participants. Completed in 16 July 2022.

Timeline
10 October 2021
Primary endpoint
16 July 2022
16 July 2022

Quick facts

Lead sponsorCairo University
PhasePhase 2, PHASE3
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingdouble
Primary purposeprevention
Enrollment30
Start date10 October 2021
Primary completion16 July 2022
Estimated completion16 July 2022
Sites1 location across Egypt

Drugs / interventions tested

Conditions studied

Sponsor

Cairo University

Who can join

Adults 1 to 5, any sex, with Burn Shock. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Effect of pre-emptive intravenous immunoglobulin administration on the incidence of septic episodes in pediatric burn patients: A randomized controlled study.

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:

Other trials of intravenous immunoglobulin

Trials testing the same drug.

Other Cairo University trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

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