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Table 1 Baseline characteristics of study subjects

From: 17-Hydroxyprogesterone caproate to prolong pregnancy after preterm rupture of the membranes: early termination of a double-blind, randomized clinical trial

 

17-Hydroxyprogesterone Caproate

Placebo

 

(N = 4)

(N = 8)

Maternal Age (years)

28 ± 3

33 ± 6

Gestational Age at PROM (weeks)

25 ± 7

26 ± 4

Gestational Age at Randomization (weeks)

28 ± 3

27 ± 3

   23.0-25.9 wks

1 (25%)

4 (50%)

   26.0-28.9 wks

1 (25%)

1 (12.5%)

   29.0-31.9 wks

2 (50%)

3 (37.5%)

Interval from PROM to Randomization (days)

3 (1-79)

1.5 (0-29)

Prepregnancy Weight (pounds)

157 ± 35

162 ± 37

Body Mass Index (kg/M2)

24 ± 7

27 ± 6

Body Mass Index > 30 kg/M2

1 (25%)

3 (37.5%)

Nulliparous

3 (75%)

5 (62.5%)

History of Prior Preterm Birth

0

0

Progestins Used Prior to 15 Weeks

1 (25%)

2 (25%)

Conception

   Spontaneous

3 (75%)

7 (87.5%)

   In Vitro Fertilization

1 (25%)

0

   Intrauterine Insemination

0

1 (12.5%)

Married/Living with Partner

3 (75%)

7 (87.5%)

College Education or More

1 (25%)

5 (62.5%)

Ethnicity

   Caucasian

3 (75%)

6 (75%)

   African-American

1 (25%)

1 (12.5%)

   Native American

0

1 (12.5%)

Reported Antepartum Substance Use

   Alcohol, Rare

0

1 (12.5%)

   Marijuana

1 (25%)

1 (12.5%)

   Tobacco

0

2 (25%)

   Other

0

0

  1. Results expressed as Mean ± SD, Median (range), or N (%).