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. 2021 Oct 20;64(6):484–495. doi: 10.5468/ogs.21264

Table 1.

The baseline characteristics of patients in the included studies

Study Country Recruitment period (weeks) Group N Age (yr) 17OHPC dose Type of treatment in control group Period of 17OHPC use (weeks) Cervical length at enrollment (mm)
Blackwell et al. [16] (2020) USA 160/7 to 206/7 weeks 17OHPC 1,130 30.0±5.2 250 mg IM weekly Placebo 16 to 36 Non-selected
Control 578 29.2±5.2

Ibrahim et al. [13] (2010) Egypt Second trimester (weeks not specified) 17OHPC 25 25.3±4.15 250 mg IM weekly Placebo 14 to 36 Non-selected
Control 25 25.6±3.85

Jafarpour et al. [17] (2020) Iran 160/7 17OHPC 50 25.4±2.6 250 mg IM weekly No placebo 16 to 37 >30
Control 50 25.0±2.38

Meis et al. [12] (2003) USA 16+0 to 20+6 weeks 17OHPC 310 26.0±5.6 250 mg IM weekly Placebo 16 to 36 Non-selected
Control 153 26.5±5.4

Berghella et al. [23] (2010) USA 16+0 to 22+6 weeks 17OHPC 52 26.3±4.5 250 mg IM weekly No placebo 16 to 36 <25
Control 100 26.8±5.3

Saghafi et al. [11] (2011) Iran 16 weeks 17OHPC 50 28.98±5.36 250 mg IM weekly No placebo 16 to 37 Non-selected
Control 50 29.32±5.69

Values are presented as mean±standard deviation unless otherwise indicated.

17OHPC, 17-alpha hydroxyprogesterone caproate; IM, intramuscularly.