Brisbois 201130
|
parallel-group RCTs |
advanced cancer patients |
THC (2.5 mg, n = 24) |
Placebo (n = 22) |
19 |
Appetite, AEs, QOL |
Johnson 201028
|
parallel-group RCTs |
advanced cancer patients |
THC:CBD extract (2.7 mg THC and 2.5 mg CBD, n = 60), THC extract (2.7 mg THC, n = 58) |
Placebo (n = 59) |
14 |
Appetite, AEs, QOL |
Strasser 200631
|
parallel-group RCTs |
advanced cancer patients |
CE (standardized for 2.5 mg THC and 1 mg cannabidiol, n = 95) or THC (2.5 mg, n = 100) |
Placebo (n = 48) |
42 |
Body weight, appetite, AEs, QOL |
NCT03245658 |
Crossover Assignment |
pancreatic cancer patients |
THC 25mg/ml and CBD 50mg/ml (n=32) |
N/A |
4 weeks |
Energy and protein intake, lean body mass, appetite, mortality, QOL |
NCT02802540 |
parallel-group RCTs |
Non-small cell lung cancer (NSCLC) patients |
1 mg nabilone |
placebo |
8 weeks |
Anorexia, percentage weight loss, body mass index, subjective global assessment, QOL, AEs |
Jatoi 200232
|
Crossover Assignment |
advanced cancer patients |
(1) megestrol acetate 800 mg/d plus placebo, (2) dronabinol 2.5 mg twice a day plus placebo, or (3) both agents |
N/A |
4 weeks |
weight, appetite, AEs, QOL |
Cote 201633
|
parallel-group RCTs |
squamous cell carcinoma patients |
0.5 mg nabilone |
placebo |
4 weeks |
QOL, pain, nausea, appetite, AEs |