Cannabis Cigarettes Used for Doping: Delta-9-Tetrahydrocannabinol (THC) Urine Detection

This study has been completed.
Sponsor:
Information provided by:
Federal Office of Sports, Switzerland
ClinicalTrials.gov Identifier:
NCT00534716
First received: September 24, 2007
Last updated: May 6, 2008
Last verified: May 2008

September 24, 2007
May 6, 2008
September 2007
December 2007   (final data collection date for primary outcome measure)
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Complete list of historical versions of study NCT00534716 on ClinicalTrials.gov Archive Site
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Cannabis Cigarettes Used for Doping: Delta-9-Tetrahydrocannabinol (THC) Urine Detection
Cannabis and Doping - Pharmacokinetics of Smoked Cannabis Under Controlled Clinical Conditions

The purpose of this study on volunteers is whether THC and short-living metabolites are suited to detect recent Cannabis smoking within urine doping control.

About half of all positive doping cases in Switzerland have been related to Cannabis consumption (mainly recreational smoking). So far, the target analyte in urine is 11-nor-9-carboxy-THC (THC-COOH), the main metabolite of delta-9-tetrahydrocannabinol (THC), which is excreted up to several days after single use. However, the wide detection window of THC-COOH does not allow a conclusion concerning the impact on the physical performance. Therefore, the evaluation of other target analytes with shorter elimination half-lives is needed and the aim (primary endpoints) of the present study. This pharmacokinetic, open, 1-session trial on 12 healthy, male, infrequently Cannabis smoking volunteers is focussed on the GC/MS profiling of THC and metabolites in urine and plasma after standardized smoking of a single 7% THC Cannabis cigarette of the Dutch Ministry of Health, Welfare & Sport, Office of Medicinal Cannabis. Pharmacodynamic measurements (secondary endpoints) include the side-effects monitoring by using Visual Analog Scales and checking vital functions.

Observational
Time Perspective: Prospective
Not Provided
Retention:   Samples Without DNA
Description:

Plasma, urine

Non-Probability Sample

Healthy male subjects; light (max. 1/month), infrequent Cannabis smokers, medium (max. 15/month) tobacco smokers experienced in the inhalation technique; age 20-30 years; body weight 75+/-15 kg, normal medical history physical examination, passed laboratory tests (safety lab), normal lung functions (spirometry).

Healthy
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*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
12
May 2008
December 2007   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • Healthy male subjects; light (max. 1/month), infrequent Cannabis smokers, medium (max. 15/month) tobacco smokers experienced in the inhalation technique; age 20-30 years; body weight 75+/-15 kg; evaluation based on normal medical history, physical examination, laboratory tests (safety lab), normal lung functions (spirometry).
  • Informed consent after information (written) by the study physician and principal investigator on nature, significance and scope of the trial.
  • Informed consent by the volunteer regarding transmitting trial-related data to the sponsor and to the competent control authorities.

Exclusion Criteria:

  • Hypersensitivity to cannabinoids. - Regular (more than once per month, weekly or daily) Cannabis use. - The use of alcohol, any medication or drugs, especially Cannabis, within the last 2 days prior to and during the 1-day session is not allowed. Cannabis use is also not allowed during the following 11 days of urine collection, i.e. up to the end of the study.
  • Positive Cannabis urine test before the session.
  • Driving any vehicle, and operating with machines during and within 48 h after the session.
  • Psychotic or vulnerable subjects.
Male
20 Years to 30 Years
Yes
Contact information is only displayed when the study is recruiting subjects
Switzerland
 
NCT00534716
KEK-33/07
Yes
Matthias Kamber, PhD, Federal Office of Sports, Office for Doping Control
Federal Office of Sports, Switzerland
Not Provided
Principal Investigator: Rudolf Brenneisen, PhD, Prof University of Bern, Dept. Clinical Research
Federal Office of Sports, Switzerland
May 2008

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP