CompletedNot applicableNCT01673711
Official study title

Deuterated Phenanthrene Tetraol in Smokers Who Are at High Risk For Lung Cancer

Study summary

This clinical trial studies deuterated phenanthrene tetraol in smokers who are at high risk for lung cancer. Studying samples of urine in the laboratory from smokers who are at high risk for lung cancer may help doctors learn more about biomarkers related to cancer.

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Key things to know

Main goalNot specified

This describes the study’s primary purpose.

What is being studieddeuterated phenanthrene tetraol and pharmacological study

Plus 1 other study approaches.

Who it may be forLung Cancer · Squamous Lung Dysplasia

These are broad labels—not an eligibility decision.

Checked against the public recordLast updated Oct 9, 2019 · Source: ClinicalTrials.gov

Is enrollment open?Completed

Ask the study team to confirm whether enrollment is open.

What kind of study?Not applicable

Observational

Where is it offered?3 U.S. locations

Locations may change over time.

Who runs it?University of Minnesota

Study sponsor

01
Study overview

What this study is about

Purpose
Not specified
Study type
Observational
Phase
Not applicable
Sponsor
University of Minnesota
Interventions being studied
Drug: deuterated phenanthrene tetraol; Drug: pharmacological study; Drug: laboratory biomarker analysis
02
Explore related studies

How this study is categorized

These labels come from structured fields and exact terms in the public record.

03
Public criteria

Who may be able to participate

The sponsor separates these requirements into two groups. You do not need to interpret them alone—use them to guide a conversation with the study team.

Requirements people may need to meetInclusion criteria
  • Current or former smoker
  • 18 years of age or older
  • Documentation of a diagnosis of no dysplasia, dysplasia, or metaplasia on bronchoscopy (white light and/or autofluorescence) conducted less than or equal to 10 years prior to registration
  • Not pregnant or breastfeeding
  • Able to provide written informed consent indicating an understanding of the nature of the study
  • Willing to comply with study requirements, including taking \[D10\]phenanthrene in water with 20% ethanol
  • No previous history of aerodigestive cancer
  • Not currently undergoing treatment for any cancers. Exception: basal cell or squamous cell skin cancer
  • Not currently taking any other investigational agents
  • No history of allergic reaction to \[D10\]phenanthrene or similar compounds
  • No major medical comorbidities, for example, renal dysfunction, heart function, and diabetes, to be adjudicated by study physicians
  • Not a former or recovering alcoholic
  • No use of metronidazole or antabuse less than or equal to 7 days prior to \[D10\]phenanthrene dosing, as they could potentially interact with ethanol

Important: This is the sponsor’s public criteria, not a determination of eligibility. The study team must review your individual situation.

04
Study sites

U.S. locations

  • Mayo ClinicRochester, Minnesota
  • Roswell Park Cancer InstituteBuffalo, New York
  • BC Cancer AgencyVancouver, British Columbia

Source and freshness
Processed from ClinicalTrials.gov. Last public update: Oct 9, 2019. Always confirm current availability with the study team.

View original record ↗