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CompletedNCT06949605Updated Mar 25, 2026

Quantitative Xylazine Measurement in ED

An observational study in Opioid Overdose and Substance Use Disorders, sponsored by Icahn School of Medicine at Mount Sinai. Completed at 2 sites in United States. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-03-25.

Sponsored by Icahn School of Medicine at Mount Sinai · Observational

Study type
Observational
Model
Cohort
Time perspective
Retrospective
Enrollment
75
Ages
18 Years and older
Sex
All
01

Study summary

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

Read the detailed 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.

02

Conditions studied

  • Opioid Overdose
  • Substance Use Disorders

Keywords

  • Opioid
  • Xylazine
  • Substance Use
03

In context

Opiate Overdose

70 studies on the registry are indexed under Opiate Overdose; 11 are open to participants now.

This study's enrollment of 75 is below the median of 284 across 16 observational studies indexed under Opiate Overdose.

Browse Opiate Overdose studies →

Lead sponsor

Icahn School of Medicine at Mount Sinai is the lead sponsor of 776 studies on the registry; 176 are open to participants now.

Of its 125 completed or terminated interventional studies of FDA-regulated products, 83 (66%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

All participating sites will enroll all opioid ODs presenting to Mount Sinai Hospital and Elmhurst Hospital Emergency Departments, regardless of whether or not a consultation by a medical toxicologist was requested (i.e., all consecutive opioid ODs).

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

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

Exclusion Criteria:

- Children under 18

05

Study design

Observational model
Cohort
Time perspective
Retrospective
Enrollment
75 participants (actual)
Patient registry
No
Biospecimen retention
Samples with dna

Groups and cohorts

  • Suspected Opioid Overdose

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

06

What researchers measure

Primary outcomes

  1. Xylazine Concentration in Blood

    Concentration of Xylazine in blood as determined by lab.

    Time frame: 6 months

Secondary outcomes

  1. Xylazine Strip Specificity and Sensitivity

    Measuring Xylazine test strip specificity and sensitivity using excess urine samples.

    Time frame: 6 months

07

Study locations

2 sites
  • NYC Health + Hospitals/Elmhurst
    Elmhurst, New York 11373, United States
  • Icahn School of Medicine
    New York, New York 10029, United States
08

References and documents

Individual participant data

Plan to share: No — Not a clinical trial

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 25, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06949605
Responsible party
Jennifer Love (Assistant Professor, Icahn School of Medicine at Mount Sinai) — Principal investigator
First posted
Apr 29, 2025
Start date
Apr 1, 2025
Primary completion
Feb 28, 2026
Completion
Feb 28, 2026
Last update
Mar 25, 2026

Study contacts

Jennifer Love, MD, MS
principal investigator · Icahn School of Medicine

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Mar 2026. You cannot join it, but the record below documents what was studied.

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