Recruiting NCT07192887

Thebaine Urine Testing

— Observational Urine Specimen Collection

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied: This is an observational study: the protocol does not assign a study treatment.
Who it may be relevant to: Registry conditions: Urine Specimen Collection. Basic parameters: 18 years — 65 years · All.
What needs checking: Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place: United States
Next step: Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Official title

Clinical Feasibility of Thebaine Urine Mass Spectrometry Drug Testing

To develop and validate a urine drug screen to detect thebaine.

Validate thebaine urine screen [Time frame: Enrollment to 48 hours after enrollment]

Allergy to poppy seeds, or any of the related food stuffs used in the study
Celiac disease or gluten sensitivity
Ongoing or opioid use in the past 6 months
History of renal or hepatic disease or dysfunction
Inability or unwillingness to give repeated urine specimens
Unwillingness to refrain from eating poppy seed-containing products during the two-day course of the study
Non-English speakers (due to study materials being in English)
BMI greater than 30
Antibiotic use in the previous 2 months
Recent ingestion of poppy seeds from the previous 7 days

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

United States · 1 center

NCT: NCT07192887 · 2024-0818