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Clinical Trials/NCT01249339
NCT01249339CompletedPhase 1

In-vivo Extraction of Lead, Cadmium and Tobacco Specific Nitrosamines From Four Brands of Swedish 'Snus' in Regular Snus Users

Contract Research Organization el AB2 sites in 1 country32 target enrollmentStarted: May 1, 2004Last updated:
Conditions

Trial Snapshot

Phase
Phase 1
Status
Completed
Sponsor
Enrollment
32
Locations
2
Primary Endpoint
In-vivo extraction of cadmium

Study Overview

Brief Summary

In an open label, randomized, two-way cross-over study, 32 male healthy regular snus users will be given repeated doses of four different types of portion snus: "General", "Catch", "Catch Mini" and "Catch Dry Mini". Each portion of used snus will be collected and frozen (-20 oC) pending analysis of lead (Pb), cadmium (Cd), nicotine and tobacco specific nitrosamines (TSNAs). Unused snus is collected and deep frozen for analysis and calculation of extracted dose. Calculations of extracted amount of lead, cadmium, nicotine and tobacco specific nitrosamines (TSNAs) respectively, will be done for each type of snus.

Detailed Description

Comparisons:

A= "General Portion" 1 g portion snus containing approximately 8 mg nicotine per portion.

B= "Catch Licorice Portion" 1 g portion snus containing approximately 8 mg nicotine per portion.

C= "Catch Licorice Portion Mini" 0.5 g portion snus containing approximately 4 mg nicotine per portion.

D= "Catch Dry Licorice Portion Mini" 0.3 g portion snus containing approximately 4 mg nicotine per portion.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Crossover
Primary Purpose
Basic Science
Masking
Single (Participant)

Eligibility Criteria

Ages
18 Years to 50 Years (Adult)
Sex
Male
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Non-smokers, 18 to 50 years of age.
  • Habitual use of > 7 portions snus daily since minimum 1 year.
  • Healthy according to the health declaration and interview.
  • Written informed consent given.

Exclusion Criteria

  • Concurrent participation in another clinical trial.
  • History of allergy.
  • History of allergy.

Outcomes

Primary Outcomes

In-vivo extraction of cadmium

Time Frame: 30 minutes' use

Extracted amount = mean of 10 unused sachets - residual amount

Secondary Outcomes

  • in-vivo extraction of tobacco specific nitrosamines (TSNAs)(30 minutes' use)
  • In-vivo extraction of lead(30 minutes' use)
  • In-vivo extraction of nicotine(30 minutes' use)

Investigators

Sponsor
Contract Research Organization el AB
Sponsor Class
Industry

Study Sites (2)

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