Main characteristics of the included studies
Trial |
Treatments |
Patients |
Methods |
Anderson, 2002
|
Bupropion, variabledose for 48 wk
versus
Placebo
|
|
follow-up
n=105/112
|
Croft, 2002
|
Bupropion, 300 mgfor 44 wk
versus
Placebo
|
|
follow-up
n=210/213
|
Jain, 2002
|
Bupropion, variabledose for 24 wk
versus
Placebo
|
|
follow-up
n=213/209
|
Breum, 1995
|
Fluoxetine, 60 mgfor 52 wk
versus
Placebo
|
|
follow-up
n=20/20
|
Connolly, 1995
|
Fluoxetine, 60 mgfor 6 mo
versus
Placebo
|
|
follow-up
n=15/15
|
Darga, 1991
|
Fluoxetine, 60 mgfor 52 wk
versus
Placebo
|
|
follow-up
n=23/22
|
Goldstein, 1994
|
Fluoxetine, 60 mgfor 52 wk
versus
Placebo
|
|
follow-up
n=182/184
|
Gray, 1992
|
Fluoxetine, 60 mgfor 6 mo
versus
Placebo
|
|
follow-up
n=24/24
|
Marcus, 1990
|
Fluoxetine, 60 mgfor 52 wk
versus
Placebo
|
|
follow-up
n=23/22
|
Mendoza Espejo, 1995
|
Fluoxetine, 180 mgfor 6 mo
versus
Placebo
|
|
follow-up
n=0/30
|
Michelson 50wk, 1999
|
Fluoxetine, 20 mgfor 50 wk
versus
Placebo
|
|
follow-up
n=102/102
|
O�Kane, 1994
|
versus
|
|
follow-up
n=10/10
|
Bakris, 2002
|
versus
|
|
follow-up
n=278/276
|
Broom, 2002
|
versus
|
|
follow-up
n=265/261
|
Broom,, 2001
|
versus
|
|
follow-up
n=71/71
|
Davidson, 1999
|
versus
|
|
follow-up
n=668/224
|
Deerochanawong,, 2001
|
versus
|
|
follow-up
n=126/126
|
Derosa, 2003
|
versus
|
|
follow-up
n=27/23
|
Gotfredsen, 2001
|
versus
|
|
follow-up
n=16/14
|
Halpern, 2003
|
versus
|
|
follow-up
n=169/174
|
Hanefeld, 2002
|
versus
|
|
follow-up
n=195/188
|
Hauptman, 2000
|
versus
|
|
follow-up
n=210/212
|
Hill, 1999
|
versus
|
|
follow-up
n=181/188
|
Hollander, 1998
|
versus
|
|
follow-up
n=163/159
|
Karhunen, 2000
|
versus
|
|
follow-up
n=36/36
|
Kelley, 2002
|
versus
|
|
follow-up
n=274/276
|
Krempf, 2005
|
versus
|
|
follow-up
n=346/350
|
Lindgarde, 2000
|
versus
|
|
follow-up
n=190/186
|
Lucas, 2003
|
versus
|
|
follow-up
n=256/188
|
Micic, 1999
|
versus
|
|
follow-up
n=60/59
|
Miles, 2002
|
versus
|
|
follow-up
n=255/261
|
Muls, 2001
|
versus
|
|
follow-up
n=147/147
|
Naumov, 2002
|
versus
|
|
follow-up
n=15/15
|
Reaven, 2001
|
versus
|
|
follow-up
n=156/91
|
Rissanen, 2001
|
versus
|
|
follow-up
n=25/26
|
Rosenfalck, 2002
|
versus
|
|
follow-up
n=3/1
|
Rossner, 2000
|
versus
|
|
follow-up
n=244/243
|
Shi Yi, 2001
|
versus
|
|
follow-up
n=986/142
|
Sjostrom, 1998
|
versus
|
|
follow-up
n=345/343
|
Vidgren, 1999
|
versus
|
|
follow-up
n=37/38
|
Bray, 2003
|
versus
|
|
follow-up
n=75/75
|
Caterson, 2003
|
versus
|
|
follow-up
n=93/97
|
Pud�homme, 2003
|
versus
|
|
follow-up
n=33/33
|
Rissanen, 2003
|
versus
|
|
follow-up
n=123/103
|
Stenlof, 2003
|
versus
|
|
follow-up
n=135/137
|
Tonstad, 2003
|
versus
|
|
follow-up
n=178/177
|
McMahon , 2000
|
versus
|
|
follow-up
n=142/157
|
McMahon, 2002
|
versus
|
|
follow-up
n=145/72
|
Smith, 2001
|
versus
|
|
follow-up
n=142/69
|
Astrup, 0
|
versus
|
|
follow-up
n=-9/-9
|
Astrup (NN8022-1807 ), 2009
NCT00422058
|
4 liraglutide doses (1.2 mg, 1.8 mg, 2.4 mg, or 3.0 mg daily)
versus
placebo
|
obese individuals without type 2 diabetes
|
follow-up 20 weeks
n=-9/-9
Parallel groups
double blind
Europe
|
BLOSSOM, 2009
|
lorcaserin 10 mg twice daily
versus
placebo
|
obese and overweight patients
|
follow-up 1 year
n=-9/-9
Parallel groups
double blind
|
SCOUT,
|
sibutramine
versus
placebo
|
overweight or obese patients with diabetes or a history of coronary or peripheral vascular disease or stroke, along with other CV risk factors
|
follow-up
n=-9/-9
Parallel groups
double blind
|
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