Placebo Controlled Study of Sublingual Salvinorin A

In this study, our aim is to determine an active but tolerable sublingual dose (range 100 to 4000 µg) of Salvinorin A (SA) in experienced subjects. This study is an ascending-dose, placebo-controlled, single-site design in 8 Salvia-experienced subjects. Subjects will receive SA doses from 0-4000 µg. Doses will be separated by at least one day. The first two doses (0 and 100µg) will be double-blinded while the last four (250, 500, 1000, 2000 and 4000µg) will be single-blind.

Topic Healthy Subjects
Compound Placebo Salvia Divinorum
Country United States of America
Visit trial
Status Completed
Results Published
Start date 06 January 2009
End date 10 January 2010
Chance of happening 100%
Phase Not Applicable
Design Blinded
Type Interventional
Generation First
Participants 8
Sex All
Age 21- 45
Therapy No

Trial Details

In this study, our aim is to determine an active but tolerable sublingual dose (range 100 to 4000 µg) of Salvinorin A (SA) in experienced subjects. This study is an ascending-dose, placebo-controlled, single-site design in 8 Salvia-experienced subjects. Subjects will receive SA doses from 0-4000 µg. Doses will be separated by at least one day. The first two doses (0 and 100µg) will be double-blinded while the last four (250, 500, 1000, 2000 and 4000µg) will be single-blind.

NCT Number NCT01149824

Sponsors & Collaborators

California Pacific Medical Center Research Institute
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Data attribution

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