Skip to main content
. 2012 Jan 8;13:5. doi: 10.1186/1745-6215-13-5

Table 3.

Data concerning the process of obtaining ethics/IRB approval of countries participating in the FAITH trial

NL
(N = 14)
CA
(N = 11)
US
(N = 19)
P-value
Time necessary for ethics/IRB approval1 (days) 104
(74-135)
55
(27 - 77)
53
(44 - 105)
0.027+ a
Revision rounds1 1 (0.0 - 1.0) 1 (0.8 - 1.0) 1 (1.0 - 3.0) 0.014+ b
Type of revisions requested:
 Wording of IC Form2 6 (42.9) 5 (50.0) 12 (66.7) 0.382++
 Content of IC Form2 6 (42.9) 5 (50.0) 8 (44.4) 0.938++
 In- or exclusion criteria2 0 (0.0) 1 (10.0) 1 (5.3) 0.511++
 Wording of study protocol2 0 (0.0) 1 (10.0) 0 (0.0) 0.185++
 Content of study protocol2 1 (7.1) 2 (20.0) 1 (5.3) 0.406++
 Additional information in study protocol/procedures2 5 (35.7) 3 (30.0) 7 (36.8) 0.932++
 Financial aspects -
Request for extra information2
0 (0.0) 1 (10.0) 3 (15.8) 0.303++
 Request additional documents2 2 (14.3) 0 (0.0) 3 (15.8) 0.421++

NL, the Netherlands; CA, Canada; US, United States.

Numbers in the headers represent the number of sites per country for which data were available.

IC, informed consent form.

1 Data are presented as median with P25-P75 given between brackets. 2 Data are presented as number with percentages.

+ Kruskal-Wallis ANOVA, ++ Chi-squared test

Post-hoc pair wise comparisons were performed using the Mann-Whitney U-test: a Statistical significance was reached when comparing NL vs. CA (p = 0.025), and NL vs. US (p = 0.019), CA vs. US: not significant. b Statistical significance was reached when comparing NL vs. US (p = 0.007), other groups: not significant