Adduct Dipstick for Diagnosis of Acetaminophen Toxicity
This trial has been completed.
|Sponsor||Arkansas Children's Hospital Research Institute|
|Collaborator||University of Arkansas|
|Start date||August 2011|
|End date||December 2015|
|Trial size||120 participants|
|Trial identifier||NCT01575847, Acetaminophen Adduct Dipstick|
This study is a non-intervention, clinical study to test "research use only" APAP protein adducts dipsticks in human blood samples. The study will be conducted in two phases. In phase 1, the research use only dipsticks and dipstick testing components will be tested for feasibility in the emergency department at UAMS. Patients will be enrolled that are having an acetaminophen level obtained as part of their medical evaluation. In phase 2, the research use only dipsticks will be tested in centers that participate in the Acute Liver Failure Study Group (ALFSG), a clinical research network funded by the National Institutes of Diabetes, Digestive and Kidney Diseases (NIDDK). Subjects participating in the clinical registry of the ALFSG will be approached for enrollment. These patients all have the diagnosis of acute liver failure or acute liver injury from a variety of etiologies, including APAP. A single blood sample will be obtained and will be aliquoted for 1) testing by the dipstick and 2) testing by high performance liquid chromatography with electrochemical detection (HPLC-EC) analysis for APAP protein adducts. APAP levels will also be determined from the second aliquot of blood. In both Phase 1 and Phase 2, the dipsticks will be read manually and by dipstick readers by independent testers that are not directly involved in the clinical care of the patients. The results of the two dipstick readings will be recorded, will remain confidential and will not be used in the diagnosis or management of the patient. The results of the dipsticks and HPLC-EC assays will be compared to the final patient diagnoses.
Accuracy of dipstick compared to HPLC-EC Method for detecting assays
time frame: Each subject will have one sample taken but chart review could last entire hospitalization expected average of 2 weeks
Male or female participants at least 12 years old.
Part 1 Inclusion Criteria: - Subject is 12-18 years of age. - Subject has an APAP level ordered as part of clinical management. Exclusion Criteria: - Previous recent history of APAP overdose in the previous 30 days. Part 2 Inclusion Criteria: - Subject is 18 years of age or older. - Subject is enrolled in the ALFSG registry.
|Official title||Adduct Dipstick for Diagnosis of Acetaminophen Toxicity|
|Principal investigator||Henry Farrar, MD|
Call for more information