TABLE 1.
Summary of characteristics of 11 included datasets (including a total of n = 3539 individuals; n = 3497 with eligible data for inclusion in IPD meta-analysis)1.
| Author/y of key publication | No. of participants (n) | Region or province | Study design | Study population | Other publications from dataset1 |
|---|---|---|---|---|---|
| Charles et al. 2011 [19] 2 | 35 | Kandal | Longitudinal trial | Nonpregnant females >16 y | |
| Charles et al. 2015 [20] 3 | 173 | Kandal | Cross-sectional | Nonpregnant females 16 y and older | |
| Fischer et al. 2023 [21] | 480 | Kampong Thom | Double-blind, 3-arm, placebo-controlled noninferiority trial | Nonpregnant females of reproductive age (18–45 y) | |
| Gallant et al. 2021 [22] | 334 | Kampong Thom | Double-blind, 4 parallel-arm randomized controlled dose-response trial | Mother (18–45 y) whose most recent pregnancy was normal, with a singleton infant born without complications | |
| Karakochuk et al. 2015 [12] | 450 | Prey Veng | Cross-sectional | Females of reproductive age (18–45 y, n = 420 nonpregnant, n = 30 pregnant) | Karakochuk et al. 2015 [29] Michaux et al. 2019 [30] Williams et al. 2020 [31] |
| Karakochuk et al. 2017 [23] | 807 | Kampong Chhnang | 2 × 2 factorial, double-blind, placebo-controlled randomized trial | Anemic nonpregnant females of reproductive age (18–45 y with Hb concentration ≤117 g/L based on HemoCue finger-prick blood sample) | Cochrane et al. 2020 [32] Karakochuk et al. 2017 [33] Pei et al. 2021 [34] Pei et al. 2023 [35] Steele et al. 2019 [36] Williams et al. 2020 [31] |
| Makurat et al. 2016 [24] | 217 | Phnom Penh | Cross-sectional | Nonpregnant nulliparous females aged <31 y | Makurat et al. 2019 [37] |
| Mlewa et al. 2025 [25] | 90 | Prey Veng | Cross-sectional | 3–8 mo pregnant with a singleton fetus | |
| Rappaport et al. 2017 [26] | 326 | Preah Vihear | Parallel, 3-arm, randomized controlled trial | Nonpregnant females of reproductive age (18–49 y) with mild-to-moderate anemia (Hb 80–119 g/L based on HemoCue capillary blood sample) | |
| Whitfield et al. 2017 [27] | 175 | Prey Veng | Double-blind, 3 parallel-arm randomized controlled efficacy trial | Nonpregnant female aged 18–45 y with ≥1 child aged 12–59 mo | |
| Wieringa et al. 2016 [28] | 452 | National | Nationwide, cross-sectional survey | Females 15–49 y (n = 445 nonpregnant, n = 7 pregnant) |
Abbreviations: Hb, hemoglobin; IPD, individual participant data.
References for conference abstracts (n = 2) and clinical trials (n = 3) registries are not included in the table. Williams et al. 2020 [31] is listed twice in the table, as it uses data from both Karakochuk et al. 2015 [12] and Karakochuk et al. 2017 [23].
Only a subset of participants from this dataset were included in our review (i.e., those in the control group with data available for ferritin and C-reactive protein) as the other participants did not meet our eligibility criteria for inclusion. In addition, those outside of our age eligibility window (15–49 y) were excluded.
Participants outside of our age eligibility window (15–49 y) were excluded.