Treatment of Acetaminophen Toxicity With N-acetylcysteine

NCT00725179 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 130

Last updated 2011-09-09

No results posted yet for this study

Summary

Retrospective chart review of patients who received N-acetylcysteine for APAP toxicity to assess length of oral vs IV treatment and overall healthcare costs.

Conditions

  • Acetaminophen Toxicity

Sponsors & Collaborators

  • Akron Children's Hospital

    lead OTHER

Principal Investigators

  • Martha Blackford, PharmD · CHMCA

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2008-08-31
Primary Completion
2008-09-30
Completion
2008-10-31

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00725179 on ClinicalTrials.gov