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Quantitative Xylazine Measurement in ED

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Mount Sinai Health System

Status

Enrolling

Conditions

Opioid Overdose
Substance Use Disorders

Study type

Observational

Funder types

Other
NIH

Identifiers

NCT06949605
5R25DA058490-02 (U.S. NIH Grant/Contract)
STUDY-24-01068

Details and patient eligibility

About

Quantitative Xylazine Measurement Among Non-Fatal Opioid Overdose (OD) Patients in the Emergency Department (ED)

Full description

Xylazine, a veterinary medication and alpha-2 agonist drug with clinical effects including prolonged sedation and skin/soft tissue wounds, has been increasingly detected with fentanyl in the illicit opioid supply. Due to its rapid emergence, limited knowledge exists regarding xylazine's health effects. In this proposed research, Dr. Love will measure xylazine and its metabolites in blood and urine samples using laboratory and point-of-care assays. Working at two New York City emergency departments, Dr. Love will collect waste serum and urine from opioid overdose patients to measure xylazine and its metabolite concentrations. The researcher will also perform qualitative assessment of urine samples with xylazine test strips to characterize urine xylazine detection using a harm reduction tool.

Enrollment

15 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • ED patient
  • Opioid OD (both NPS and non-NPS)
  • Availability of waste blood specimens for analysis
  • Availability of waste urine specimens for analysis

Exclusion criteria

  • Children under 18

Trial design

15 participants in 1 patient group

Suspected Opioid Overdose
Description:
Individuals presenting to the ED with a suspected Opioid Overdose with Xylazine exposure.

Trial contacts and locations

2

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Central trial contact

Jonathan Berger, MPH

Data sourced from clinicaltrials.gov

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