Author (year) | Study details | Major findings | ||
Design and subjects | Interventions | Assessment timeframes | ||
Non-pregnant women | ||||
Blanco-Rojo et al. (2011) [26] | RCT N = 122 18 - 35 years Low Fe stores (serum ferritin < 40 ng/ml) Hb ≥ 110 g/l | microencapsulated iron pyrophosphate (F group, n = 64) Vs placebo (P group, n = 58) as supplement to diet | 16 weeks | Compared to P, F resulted in significant improvement of - total erythrocyte count (p = 0.046), - hematocrit (p = 0.006) - RDW (p = 0.003) - Hb (p < 0.0001) - serum ferritin (p < 0.0001) - sTfR (p = 0.01) |
Pleşea-Condratovici et al. (2012) [27] | Open label N = 30 Post-menopausal 45 - 65 years Hb < 11.5 gm/dL Previous side effects with iron supplements Intervention: | microencapsulated iron pyrophosphate in liposomal form | 8 weeks | Liposomal iron supplementation was associated with significant increase in - Hb levels (p < 0.0001) - Hematocrit levels (P < 0.0001) - no dropouts - well tolerated: significant improvement was reported in all the side effects previously experienced by the patients |
Pregnant women | ||||
Parisi et al. (2012) [28] | RCT N = 80 Non-anemic | Group 1: FF14: Liposomal iron 14 mg/d Group 2: FF28: Liposomal iron 28 mg/d Group 3: SF: ferrous sulphate 30 mg/d Group 4: C: control | At 20 weeks, 28 weeks and 6 weeks post-partum | FF28 was associated with - significant improvement of Hb (p < 0.01 vs SF and < 0.05 vs C) at 28 weeks and in post-partum period - significant improvement of ferritin levels than control at 20 weeks (p = 0.05), 28 weeks (p < 0.01) and in post-partum period (p < 0.01) - lower drop outs (n = 2) than SF (n = 5) and C (n = 6) - significantly higher birth weight (p < 0.05 vs C) |
Parisi et al. (2012) [29] | RCT N = 55 Anemic (Hb < 10.5 gm%) | Group 1: Fe sulphate 30 mg (FeS 30, n = 13) Group 2: Liposomal ferric pyrophosphate 14 mg (FeP 14, n = 12) Group 3: Liposomal ferric pyrophosphate 28 mg (FeP, 28, n = 11) Group 4: control group with no supplementation (C, n = 19) | At 28 weeks, After delivery | FeP28 treatment was associated - significantly greater increase in Hb compared to control (p < 0.01) at 28 weeks (with no other group having significant difference compared to control) - no development of siderophenic anemia compared to women in control (n = 5), FeS (n = 2) and FeP14 (n = 1) groups |