Authors | Year | Drug | Type of study | Patients (N) | Treatment scheme | Definite cure (95Â % CI) | Reference |
---|---|---|---|---|---|---|---|
Thakur et al. | 1991 | SSG and Pentamidine | Randomised controlled comparative trial | 312 | Group-1 : Pentamidine (i.v) 4Â mg/kg/day three times weekly until parasitological cure was achieved | Group 1:78Â % Group 2: 84Â % Group 3: 98Â % | [128] |
Group-2: Pentamidine (i.v) 4 mg/kg/day three times weekly + SSG (i.m) 20 mg/kg/day for 20 days | |||||||
Group-3: Pentamidine (i.v) 4 mg/kg/day three times weekly until parasitological cure was achieved + SSG (i.m) 20 mg/kg/day for 20 days | |||||||
Thakur et al. | 1992 | Paramomycin and SSG | Non comparative study | 22 | Paramomycin (i.v) 12Â mg/kg/day + | 81.8Â % | [47] |
SSG (i.m) 20Â mg/kg/day for 20Â days | |||||||
Thakur et al. | 2000 | SSG and Paramomycin | Randomized comparative study | 149 | Group 1: Paramomycin 12 mg/kg/day + SSG (i.m) 20 mg/kg/day for 21 days | Group 1:92.3 % Group 2: 93.8 %, Group 3: 53.1 % | [141] |
Group 2: Paramomycin 18 mg/kg/day + SSG (i.m) 20 mg/kg/day for 20 days | |||||||
Group 3: SSG (i.m) 20Â mg/kg/day for 21Â days | |||||||
Das et al. | 2001 | Pentamidine and Allopurinol | Randomized controlled comparative trial | 158 | Group 1: Pentamidine (i.m) 2 mg/kg/day on alternate days + allopurinol (oral) 15 mg/kg/day for 30 days | Group 1: 91.2 %, Group 2: 74.3 % | [67] |
Group 2: : Pentamidine (i.m) 2Â mg/kg/day on alternate days for 30Â days | |||||||
Sundar et al. | 2008 | L-AmB and Miltefosine | Randomized non-comparative, group sequential | 226 | Group1: L-AmB (i.v) 5 mg/kg single dose | Group 1: 91 % (78–97); | [142] |
Group 2: L-AmB (i.v) 5 mg/kg single dose + miltefosine 100 mg/day for 10 days | Group 2: 98 % (87–100); | ||||||
Group3: L- AmB (i.v) 5 mg/kg single dose + miltefosine 100 mg/day for 14 days | Group 3: 96 % (84–99); | ||||||
Group 4: L-AmB (i.v) 3.75 mg/kg single dose + miltefosine 100 mg/day for 14 days | Group 4: 96 % (84–99); | ||||||
Group 5: L-AmB (i.v) 5 mg/kg single dose + miltefosine 100 mg/day for 7 days | Group 5: 98 % (87–100) | ||||||
Sundar et al. | 2010 | L-AmB, Miltefosine | Non-randomized multicentric trial | 135 | L-AmB (i.v) 5 mg/kg for single dose + miltefosine (oral) 2.5 mg/kg/day for 14 days | 91.9 % | [143] |
Sundar et al. | 2011 | AmB, L-AmB, Paramomycin, Miltefosine | Open label non-inferiority randomized control trial | 634 | Group 1: AmB (i.v) 1 mg/kg on alternate days for 30 days | Group 1: 93 % (88–96); | [144] |
Group 2: L-AmB (i.v) 5 mg/kg for single dose + miltefosine (oral) 50 mg/kg for 7 days | Group 2: 98 % (93–99) | ||||||
Group 3: Paramomycin (i.m) 11 mg/kg/day for 10 days | Group 3: 98 % (93–99); | ||||||
Group 4: Miltefosine (oral) 50 mg/day for 10 days + paramomycin (i.m) 11 mg/kg/day for 10 days | Group 4: 99 % (95–100); |