
TABLE 2. Clinical trials of clindamycin plus quinine against P. falciparum malaria
Study details
|
Regimen
|
Efficacy (%) |
Reference |
| Yr |
Place |
Designb |
Pop.c |
Nd |
Clindamycin
|
Quinine
|
Routee |
Days |
Dosingf |
| Dosage, forma |
No. of doses/day |
Dosage |
No. of doses/day |
|
| 1974 |
United States |
WHO |
A |
5 |
450 mg, salt |
4 |
540 mg |
3 |
p.o. |
3 |
Yes |
100 |
43 |
| 1975 |
United States |
WHO |
A |
5 |
450 mg, salt |
3 |
560 mg |
3 |
p.o. |
3 |
Yes |
60 |
11 |
| 1975 |
United States |
WHO |
A |
2 |
600 mg, salt |
1 |
560 mg |
3 |
p.o. |
3 |
No |
50 |
11 |
| 1975 |
Thailand |
WHO |
A |
4 |
450 mg, salt |
3 |
540 mg |
3 |
p.o. |
3 |
Yes |
100 |
20 |
| 1975 |
Thailand |
WHO |
A |
5 |
150 mg, salt |
3 |
270 mg |
3 |
p.o. |
3 |
No |
60 |
20 |
| 1988 |
Brazil |
WHO, RCT |
A |
40 |
10 mg/kg, base |
2 |
12 mg/kg |
2 |
p.o. |
3 |
Yes |
90 |
28 |
| 1994 |
Gabon |
WHO, RCT |
C |
34 |
5 mg/kg, base |
2 |
12 mg/kg |
2 |
p.o. |
3 |
Yes |
88 |
32 |
| 1995 |
Gabon |
WHO, RCT |
Cg |
50 |
5 mg/kg, base |
3 |
8 mg/kg |
3 |
i.v. |
4 |
Yes |
96 |
31 |
| 1995 |
Gabon |
WHO, RCT |
A |
40 |
5 mg/kg, base |
2 |
12 mg/kg |
2 |
p.o. |
3h |
Yes |
92 |
41 |
| 1997 |
Gabon |
WHOi |
C |
161 |
8 mg/kg, salt |
2 |
8 mg/kg |
2 |
p.o. |
3 |
Yes |
97 |
62 |
| 2000 |
Thailand |
WHO, RCT |
A |
68 |
5 mg/kg, base |
4 |
8 mg/kg |
3 |
p.o. |
7 |
Yes |
100 |
50 |
| 2001 |
France |
WHO, RCT |
A |
53 |
5 mg/kg, salt |
3 |
8 mg/kg |
3 |
i.v. |
3 |
Yes |
100 |
45 |
| 2001 |
Thailand |
WHO, RCT |
P |
65 |
5 mg/kg, NSj |
3 |
8 mg/kg |
3 |
p.o. |
7 |
Yes |
100 |
37 |
|
a Eight milligrams of clindamycin hydrochloride salt is equivalent to 5 mg of base.
b WHO, study conducted according to World Health Organization guidelines (67); RCT, randomized controlled trial.
c Pop., study population; A, adults; C, children; P, pregnant women.
d N, number of subjects.
e i.v., intravenous; p.o., oral.
f Adaequate dosing (i.e., clindamycin given at least twice daily and more than 3 days).
g Severe malaria.
h Quinine was administered for only 1.5 days.
i Short follow-up (3 weeks).
j NS, not specified.