Skip to main content
. Author manuscript; available in PMC: 2021 Sep 1.
Published in final edited form as: Contraception. 2020 May 19;102(3):168–173. doi: 10.1016/j.contraception.2020.05.004

Table 2.

Spotting and bleeding and bothersome assessment in the first month of using a contraceptive vaginal ring releasing estradiol 75 mcg, 100 mcg, or 200 mcg per day and segesterone acetate 200 mcg per day

E2 75 mcg/day and SA 200 mcg/day
n=22
E2 100 mcg/day and SA 200 mcg/day
n=21
E2 200 mcg/day and SA 200 mcg/day
n=22
Week 1*ǂ
 Spotting 7 (31.8) 3 (14.3) 6 (27.3)
Bothersome 0 1 (33.3) 2 (33.3)
 Bleeding 8 (36.4) 2 (9.5) 6 (27.3)
Bothersome 0 0 3 (50.0)
Week 2*
 Spotting 4 (18.2) 5 (23.8) 1 (4.5)
Bothersome 3 (75.0) 2 (40.0) 1 (100)
 Bleeding 1 (4.5) 4 (19.0) 0
Bothersome 1 (100) 4 (100) 0
Week 3*
 Spotting 7 (31.8) 5 (23.8) 0
Bothersome 5 (71.4) 4 (80.0) 0
 Bleeding 4 (18.2) 4 (19.0) 0
Bothersome 4 (100) 2 (50.0) 0
Week 4*
 Spotting 10 (45.5) 8 (38.1) 0
Bothersome 5 (50.0) 7 (87.5) 0
 Bleeding 7 (31.8) 4 (19.0) 1 (4.5)
Bothersome 5 (71.4) 2 (50.0) 1 (100)
*

Participants reported bleeding or spotting in week prior. Bothersome assessment done in participants who reported spotting or bleeding.

ǂ

Participants initiated ring use during menses so the bleeding and spotting in week 1 include residual menses from a cycle prior to treatment.

Data presented as n (%); SA = Segesterone Acetate; E2 = estradiol