Recruiting

Observational Study

Sponsor:

Avioq, Inc.

Code:

NCT02026440

Conditions

Smoking

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Accepted

Study Details

Brief summary:

The VioOne Oral Fluid Sample Collection Device can be used to collect human oral fluid samples for detection of cotinine using an ELISA cotinine assay.

Conditions

Smoking

Study ID

NCT02026440

Start date

Dec, 2013

Status verified date

Dec, 2013

Completion date

Apr, 2014

Anticipated

Primary completion date

Mar, 2014

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Accepted

Inclusion Criteria:

  • healthy adults (aged 18 or older)

Exclusion Criteria:

  • individuals with significant health problems.

Study Design

Enrollment

250 participants

Anticipated

Interventions and Outcome Measures

Arms

Smokers

Those who smoke at least one cigarette a day.

Non smokers

Those who have not smoked for at least one week when the sample is collected.

Primary outcome measure

  • Presence of Nicotine in Collected Oral Fluid Samples [ Time Frame: Within one week of sample collection ]

Central Contacts and Locations

Locations

Avioq

Recruiting

Research Triangle Park, North Carolina, United States, 27709

Contacts

Krista Reddington, BS

919-314-5535reddingtonk@avioq.com

More Information

Sponsor

Avioq, Inc.

Last update posted

Jan 3, 2014

Last verified

Dec, 2013

Keywords

  • oral fluid collection device cotinine detection

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-10. This information was provided to ClinicalTrials.gov by Avioq, Inc. on 2014-01-03.