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. 2000 Aug 5;321(7257):329–333. doi: 10.1136/bmj.321.7257.329

Table 3.

Efficacy results measured as sustained and point prevalence reductions in smoking and point prevalence abstinence rates according to treatment with oral nicotine inhaler (active treatment) or placebo

Definition Time point (months) No (%) with active treatment No (%) with placebo Odds ratio (95% CI) P value (Fisher's test)
Sustained
 Reduction* 4 52 (26.0) 18 (9.0) 3.55 (2.04 to 6.19) <0.001
12 26 (13.0) 8 (4.0) 3.59 (1.65 to 7.80) 0.002
24 19 (9.5) 6 (3.0) 3.39 (1.39 to 8.29) 0.012
Point prevalence
 Reduction 4 83 (41.5) 44 (22.0) 2.52 (1.63 to 3.87) <0.001
12 59 (29.5) 43 (21.5) 1.53 (0.97 to 2.40) 0.085
24 55 (27.5) 46 (23.0) 1.27 (0.81 to 2.00) 0.357
Abstinence 4 13 (6.5) 4 (2.0)  3.41 (1.16 to 10.01) 0.044
12 16 (8.0) 12 (6.0) 1.36 (0.63 to 2.95) 0.557
24 21 (10.5) 17 (8.5) 1.26 (0.65 to 2.47) 0.609
*

Sustained reduction in number of cigarettes smoked daily by at least 50% from week 6, verified by decreased carbon monoxide concentrations compared with baseline. 

Point prevalence reduction of cigarettes smoked daily by at least 50% at months 4, 12, and 24, verified by decreased carbon monoxide concentrations compared with baseline. 

No cigarettes smoked, verified by carbon monoxide concentrations <10 ppm at months 4, 12, and 24.