Table 5

 Analysis of the first part of the study as a parallel-group design placebo-controlled study

Before citalopramCitalopram 3 weeksCitalopram 6 weeks3 weeks after citalopramBefore placeboPlacebo 3 weeksPlacebo 6 weeks3 weeks after placebo
*Significant compared with run in: p<0.05.
†Significant compared with placebo: p<0.05.
Only those parameters where significance was reached are shown.
No of days abdominal pain5.4 (0.3)4.8 (0.4)3.7 (0.5)*†4.0 (0.4)*5.4 (0.3)5.3 (0.3)5.2 (0.3)5.2 (0.4)
Severity of abdominal pain7.2 (0.6)6.2 (0.6)4.9 (0.7)*†5.4 (0.8)*7.8 (0.4)7.0 (0.4)7.0 (0.6)7.2 (0.8)
Worst episode of abdominal pain7.8 (0.6)6.6 (0.6)*†4.9 (0.8)*†5.4 (0.8)8.8 (0.3)8.7 (0.4)8.5 (0.4)7.7 (0.9)
No of days with bloating4.9 (0.5)4.2 (0.5)*3.4 (0.4)*4.2 (0.5)4.8 (0.5)4.5 (0.5)3.8 (0.6)4.2 (0.6)
Severity of bloating6.5 (0.8)5.1 (0.6)4.7 (0.7)*5.1 (0.7)*5.8 (0.7)5.4 (0.8)4.8 (0.7)5.2 (1.0)
Worst episode of bloating7.2 (0.9)6.6 (0.6)6.2 (0.5)6.1 (0.8)7.1 (0.8)6.2 (0.9)*7.0 (1.0)6.4 (0.9)*
No of days with incomplete evacuation3.8 (0.6)3.2 (0.4)*3.2 (0.5)*4.0 (0.5)†2.6 (0.5)2.7 (0.4)2.5 (05)2.3 (0.4)
Overall severity assessment7.1 (0.7)5.7 (0.7)*†5.0 (0.8)*†5.4 (0.9)*7.8 (0.2)7.7 (0.4)7.3 (0.5)6.8 (0.7)
No of days with impact on daily life5.2 (0.4)4.4 (0.3)*3.7 (0.5)*4.1 (0.5)*4.9 (0.2)5.0 (0.2)4.4 (0.2)4.5 (0.4)
Severity of impact on daily life6.5 (0.6)5.7 (0.7)*5.1 (0.8)*6.0 (0.7)6.9 (0.4)6.9 (0.4)6.4 (0.4)6.6 (0.7)