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. 2026 Jun 15;17(7):100681. doi: 10.1016/j.advnut.2026.100681

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.

1

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].

2

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.

3

Participants outside of our age eligibility window (15–49 y) were excluded.