The primary purpose of this study is to determine if dronabinol is effective in preventing or treating nausea caused by HAART (highly active anti-retroviral therapy) in HIV and AIDS patients
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
103
2.5 mg to 40 mg
placebo
The absence of nausea as indicated by a visual analog scale (VAS) score < 5 mm
Time frame: 2 weeks
Number of episodes vomiting/retching
Time frame: 2 weeks
Duration of nausea, vomiting/retching
Time frame: 2 weeks
Intensity of nausea by VAS
Time frame: 2 weeks
Appetite stimulation by VAS
Time frame: 2 weeks
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