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Table 2 Per-protocol crude/unadjusted and PCR-adjusted study endpoints at days 28 and 42 of patient follow-up. Patients with re-infections and individuals for whom the outcome could not be assessed by PCR were censored from the PCR adjusted analysis

From: In vivo efficacy of artesunate–amodiaquine and artemether–lumefantrine for the treatment of uncomplicated falciparum malaria: an open-randomized, non-inferiority clinical trial in South Kivu, Democratic Republic of Congo

Crude/no PCR

Day 28

Day 42

ASAQ (n = 119)

AL (n = 122)

p value

ASAQ (n = 119)

AL (n = 119)

p value

n

%

n

%

n

%

n

%

Late clinical failure

8

6.7

4

3.3

0.250

13

10.9

10

8.4

0.510

Late parasitological failure

10

8.4

6

4.9

0.277

14

11.8

9

7.6

0.273

Adequate clinical and parasitological response

101

84.9

112

91.8

0.093

92

77.3

100

84.0

0.189

Cumulative failure

18

15.1

10

8.2

0.093

27

22.7

19

16.0

0.189

PCR adjusted/corrected

Day 28

Day 42

ASAQ (n = 105)

 AL (n = 111)

p value

ASAQ (n = 98)

 AL (n = 101)

p value

n

%

n

%

n

%

n

%

Late clinical failure (recrudescence)

1

1.0

0

0

0.486

1

1.0

1

1.0

1.000

Late parasitological failure (recrudenscence)

3

2.9

0

0

0.113

5

5.1

0

0

0.027

Adequate clinical and parasitological response

101

96.2

111

100

0.038

92

93.9

100

99.0

0.049

Cumulative failure

4

3.8

0

0

0.054

6

6.1

1

1.0

0.062

  1. The analysis of the treatment outcomes by intention-to-treat are shown in Additional file 1: Annexure 1