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. 2020 Aug 17;9(9):27. doi: 10.1167/tvst.9.9.27

Table 1.

Basal Demographic and Clinical Characteristics of the Interventional Study Population

Characteristic Placebo (n = 19) 95% CI Levosulpiride (n = 18) 95% CI P
Age (y), mean ± SEM 56.6 ± 1.3 53.9–59.3 57.4 ± 1.8 53.7–61.1 0.69a
Sex F, n (%) 8 (42.1) 8 (44.4) 0.89b
BMI (kg/m2), mean ± SEM 28.1 ± 1.2 25.6–30.5 26.1 ± 1.2 23.6–28.6 0.24a
DM2 (y), mean ± SEM 17.5 ± 1.2 15.1–19.9 15.3 ± 1.6 11.9–18.6 0.26a
HbA1c (%), mean ± SEM 7.5 ± 0.3 6.8–8.2 7.8 ± 0.4 6.9–8.7 0.55a
SCr (mg/dL), mean ± SEM 1.3 ± 0.1 1.0–1.5 1.0 ± 0.08 0.9–1.2 0.08a
eGFR (mL/min), mean ± SEM 64 ± 5.7 52–75.9 76.4 ± 4.5 66.9–85.9 0.09a
SPRL (ng/mL), mean ± SEM 6.9 ± 0.8 5.2–8.6 9.3 ± 1.4 6.3–12.3 0.15a

All patients had proliferative diabetic retinopathy before undergoing elective pars plana vitrectomy and oral treatment with placebo or levosulpiride. P values compare basal values of groups receiving placebo and levosulpiride. BMI, body mass index; CI, confidence interval; DM2, type 2 diabetes mellitus; HbA1c, glycosylated hemoglobin; SCr, serum creatinine; eGFR, estimated glomerular filtration rate (CKD-EPI equation); SPRL, serum PRL.

a

Based on Student's t-test.

b

Based on χ2 test.