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. Author manuscript; available in PMC: 2013 Nov 1.
Published in final edited form as: Am J Obstet Gynecol. 2012 Aug 6;207(5):396.e1–396.e8. doi: 10.1016/j.ajog.2012.08.001

Table 1.

Characteristics of Subjects Enrolled in the Ancillary Study

17-OHPC (N=99) Placebo (N=118) P value

Maternal age (years) 29 (26–35) 30 (24–35) 0.96
Nulliparous 40 (40.4%) 55 (46.6%) 0.36
Prior preterm birth 9 (9.0%) 8 (6.8%) 0.53
Race/ethnicity 0.91
African American 24 (24.2%) 27 (22.9%)
Hispanic 14 (14.1%) 15 (12.7%)
Caucasian/other 61 (61.6%) 76 (64.4%)
BMI at enrollment 26.7 (22.5–30.5) 24.3 (21.0–28.7) 0.07
Gestational age at enrollment (weeks) 19 (18–20) 19 (18–20) 0.75
Gestational age at delivery (weeks) 35.9 (34.1–37.1) 36 (34.1–37.3) 00.76
Delivery < 37 weeks 67(67.7%) 84(71.2%) 0.58
Delivery < 34 weeks 24(24.2%) 25 (21.2%) 0.59
Monochorionic 14 (14.1%) 18 (15.3%) 0.82
Gestational age at 1st blood draw (weeks) 26.3 (25.4–27.1) 26.3 (25.6–27.0) 0.84
Number of injections by 1st blood draw 7 (6–8) 7 (6–8) 0.58
Gestational age at 2nd blood draw (weeks)* 32.7(32.3–33.6) 33.3 (32.7 – 33.9) 0.02
Number of injections by 2nd blood draw* 14 (12–15) 14 (13–15) 0.82

Values expressed as n (%) or median and interquartile range. P-values are from Chi-square or Wilcoxon tests as appropriate

*

Based on 72 women in the 17OHPC group and 92 women in the placebo group who completed all of their injections through the second blood draw