This study will evaluate the potential therapeutic value of two neurosteroid treatments (DHEA and pregnenolone) in the treatment of tobacco withdrawal symptoms. This will include assessing whether these agents relieve craving for cigarettes elicited by exposure to a mildly stressful cognitive task. Pregnenolone (400 mg orally), DHEA (400 mg orally) and placebo will be administered one at each of the three sessions in a randomized order.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Enrollment
22
one-time 400mg oral dose of DHEA
one-time 400mg oral dose of pregnenolone
one-time dose oral dose
Duke Center for Nicotine & Smoking Cessation Research
Durham, North Carolina, United States
Duke Center for Nicotine & Smoking Cessation Research
Raleigh, North Carolina, United States
The administration of DHEA or pregnenolone will reduce smoking withdrawal symptoms.
Time frame: 6 months
The administration of DHEA or pregnenolone will reduce the subjective rewarding effects of nicotine inhaled in cigarette smoke.
Time frame: 6 months
The administration of DHEA or pregnenolone will reduce stress-induced changes in mood and craving for cigarettes.
Time frame: 6 months
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