Skip to main content

Table 2 Main pharmacokinetic parameters of three drugs described by their name (overt) or as placebo (covert)

From: Does the placebo effect modulate drug bioavailability? Randomized cross-over studies of three drugs

 

Cephalexin

Ibuprofen

Paracetamol

Parameter

Overt

Covert

P value

Overt

Covert

P value

Overt

Covert

P value

AUCT (μg.hr./ml)

68.53 ± 26.39

67.20 ± 24.96

0.47

104.38 ± 20.08

101.43 ± 21.82

0.27

18.48 ± 3.98

18.52 ± 3.68

0.62

AUCI (μg.hr./ml)

71.11 ± 28.04

69.61 ± 25.77

0.46

109.40 ± 20.45

109.65 ± 21.54

0.99

19.04 ± 4.11

19.07 ± 3.79

0.65

Cmax (μg/ml)

40.16 ± 16.51

39.32 ± 17.01

0.68

31.97 ± 6.53

29.17 ± 10.34

0.08

5.72 ± 1.74

6.08 ± 1.62

0.16

Tmax (hr)

1.11 ± 0.42

1.09 ± 0.49

0.82

1.86 ± 0.90

2.02 ± 1.21

0.58

1.01 ± 0.66

0.94 ± 0.62

0.45

λ (hr −1)

0.68 ± 0.15

0.67 ± 0.13

0.99

0.39 ± 0.06

0.35 ± 0.08

0.052

0.30 ± 0.05

0.30 ± 0.05

0.51

t½ (hr)

1.07 ± 0.23

1.07 ± 0.23

0.99

1.85 ± 0.53

2.11 ± 0.74

0.052

2.33 ± 0.35

2.35 ± 0.35

0.51

Cmax/AUCI (hr −1)

0.57 ± 0.12

0.56 ± 0.12

0.86

0.30 ± 0.05

0.27 ± 0.08

0.06

0.30 ± 0.07

0.33 ± 0.10

0.14

AUCT/AUCI

0.97 ± 0.02

0.97 ± 0.02

0.84

0.95 ± 0.05

0.93 ± 0.08

0.10

0.97 ± 0.01

0.97 ± 0.02

0.74

AUCOverttmax (μg.hr./ml)

17.87 ± 10.91

19.98 ± 15.56

0.73

22.65 ± 9.84

24.69 ± 25.77

0.04

2.51 ± 2.11

3.02 ± 2.90

0.10

  1. Data are unadjusted mean±SD of untransformed values. AUCT is area-under-the-plasma-concentration-time curve from time 0 to last measured concentration. AUCI is area-under-the-plasma-concentration-time curve extrapolated to infinity. Cmax and Tmax are first measured maximum plasma level and its time, respectively. λ is terminal elimination constant. t½ is plasma half-life. AUCOverttmax is area-under-the-plasma-concentration-time curve to Tmax under overt drug administration. P values were obtained from Analysis of variance (ANOVA) of natural logarithm-transformed values except for Tmax.