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NCT07454590

Evaluation of Differences Between the Standered NAC Regimen Protocol and the SNAP Regimen Protocol in the Treatment of Paracetamol Toxicity for Cases Presented Early and Late to Assiut University Hospitals in Terms of Safety and Efficiecy.

Not yet recruiting NA Last updated 6 March 2026
What this trial tests

NA trial testing Evidence-based medical care for paracetamol toxicity in Paracetamol Toxicity in 102 participants. Not yet recruiting.

Timeline
1 April 2026
Primary endpoint
1 April 2027
1 June 2027

Quick facts

Lead sponsorAssiut University
PhaseNA
StatusNot yet recruiting
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingdouble
Primary purposetreatment
Enrollment102
Start date1 April 2026
Primary completion1 April 2027
Estimated completion1 June 2027
Sites1 location across Egypt

Drugs / interventions tested

Conditions studied

Sponsor

Assiut University

Who can join

Under 18, any sex, with Paracetamol Toxicity. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Evaluation of differences between the 21 h NAC regimen protocol and the 12 h NAC regimen protocol in the treatment of paracetamol toxicity (over dose) for cases presented early and late to Assiut University Hospitals in terms of safety and efficiecy.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other Assiut University trials

Trials by the same sponsor.

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Data sources for this page

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