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Property:Drop-out reasons

From CAMIH

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S
The safety analysis set contained 236 patients, 118 in the intervention and 118 in the placebo arm. The full analysis set (FAS) contained 225 patients, 109 in the intervention and 116 in the placebo arm. The per-protocol set (PPS) contained 203 patients, 95 in the intervention and 108 in the placebo arm.  +
The safety analysis set contained 236 patients, 118 in the intervention and 118 in the placebo arm. The full analysis set (FAS) contained 225 patients, 109 in the intervention and 116 in the placebo arm. The per-protocol set (PPS) contained 203 patients, 95 in the intervention and 108 in the placebo arm.  +
T
Not separated by arm: 3/4 (no further information obtained after randomization), 1/4 (randomized twice)  +
Not separated by arm: 3/4 (no further information obtained after randomization), 1/4 (randomized twice)  +
U
n=1 lost to follow-up within 6 month, n=23 stopped study medication (n=14 for nonmedical reasons, n=9 for medical reasons)  +