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. Author manuscript; available in PMC: 2021 Oct 1.
Published in final edited form as: Contraception. 2021 Jun 19;104(4):327–336. doi: 10.1016/j.contraception.2021.06.010

Table I –

Baseline characteristics of the study groups according to the ulipristal acetate dose released by a copper intrauterine system

Variables 5 μg UPA/d N = 10 20 μg UPA/d N = 10 40 μg UPA/d N = 9 P value

Median (IQR) *

Age (years) 34.0 (29.0–35.0) 33.0 (27.0–35.0) 31.0 (30.0–35.0) 0.15
BMI (Kg/m2) 26.3 (21.3–28.1) 24.8 (21.9–27.8) 25.3 (23.7–26.5) 0.10
Schooling (years) 9.0 (8.0–12.0) 11.0 (7.0–14.0) 11.0 (8.0–13.0) 0.34

N (%) **

Parity 0.75
 1–2 1 (10) 2 (20) 2 (22.2)
 ≥ 3 9 (90) 8 (80) 7 (77.8)
Race 0.39
 Black 1 (10) 0 0
 White 1 (10) 0 0
 Mixed 8 (80) 10 (100) 9 (100)
Ethnicity 0.99
 Latina/Hispanic 10 (100) 10 (100) 9 (100)
Marital Status 0.29
 Married/Cohabiting 10 (100) 8 (80) 7 (77.8)
 Other1 0 2 (20) 2 (22.2)
Non-smokers 10 (100) 10 (100) 9 (100) 0.99
Previous IUD use 0 1 (10) 0 0.37
Usual volume of menstrual flow 0.52
 Scanty (1–2 pads/day) 2 (20) 1 (10) 2 (22.2)
 Moderate (3–4 pads/day) 8 (80) 8 (80) 5 (55.6)
 Heavy (> 4 pads/day) 0 1 (10) 2 (22.2)
Usual duration of menses 0.43
 < 3 days 3 (30) 1 (10) 3 (33.3)
 4–7 days 7 (70) 9 (90) 6 (66.7)
*

Kruskal-Wallis test

**

Chi-Square or Fisher’s exact test

IQR: interquartile range; UPA: ulipristal acetate; IUD: intrauterine device; BMI: body mass index

1

: Includes single, divorced and other.

Intention-to-treat population included the 29 randomized participants