Table 2

Characteristics of the included randomised clinical trials

StudynOral (%)Male (%)Diabetes (%)Age IV±SDAge oral±SDCIN oral/IVHDCr IV baseline±SDCr oral baseline±SDCr IV 48 h±SDCr oral 48–72 h±SDContrast Vol IV±SDContrast Vol oral±SD
Trivedi et al55326 (49.1)52 (98.1)10 (18.9)68.5±867.2±11.29/1None1.14±0.241.27±0.371.27±0.481.60±0.83201.3±92187.3±87.6
Kong et al1112080 (66.7)67 (55.8)30 (25)55.7±11.956.05±105/2None1.15±0.291.23±0.261.27±0.311.3±0.27151.2±63.1151±59.5
Dussol et al615377 (50.3)128 (83.7)44 (28.8)64±1163±154/5None2.35±0.952.14±0.74NRNR115±57120±40
Cho et al74922 (44.9)27 (55.1)16 (32.7)77.3±8.480.8±6.51/6NR1.381.38NRNR122.6118.6
Wrobel et al810250 (49)58 (56.9)102 (100)67.3±7.7663.7±7.822/3None1.24±0.451.17±0.391.35±0.481.24±0.44101.1±36.6110.4±65.28
  • CIN, contrast-induced nephropathy; Cr creatinine; HD, hemodialysis; IV, intravenous; n, total number of participants; NR, not reported; Vol, volume.