TY - JOUR
T1 - Effect of intermittent treatment with mifepristone on bleeding patterns in Norplant® implant users
AU - Massai, María Rebeca
AU - Pavez, Margarita
AU - Fuentealba, Blanca
AU - Croxatto, Horacio B.
AU - D'Arcangues, Catherine
N1 - Funding Information:
This study was funded by the UNDPD/UNFPA/WHO/World Bank Special Programme of Research, Development and Research Training in Human Reproduction. Roussel Uclaf, Romainville, France, provided the mifepristone and placebo tablets used in this study and Leiras, Turku, Finland, the Norplant implants. The authors are grateful to the participants in the study for their sustained collaboration, to R. Ferrera for coordinating the follow-up and to A. Zepeda for her statistical advice.
PY - 2004/7
Y1 - 2004/7
N2 - A double-blind, placebo-controlled, randomized trial, was carried out in 120 Norplant® users to evaluate the effect of mifepristone, 100 mg/day administered for 2 consecutive days every 30 days, on the vaginal bleeding pattern. Treatment was given from months 2-7 of implant use. Volunteers recorded bleeding and spotting days, during treatment and for the ensuing 6-month period. During treatment, women on mifepristone recorded the same frequency of bleeding/spotting episodes but significantly less prolonged bleeding episodes than placebo controls (mean ± SD: 11 ± 3 vs. 22 ± 23 days) and their total number of bleeding days was 35% lower than in the placebo group. After the end of mifepristone use, bleeding patterns were similar in both groups. One pregnancy occurred in the mifepristone-treated group, in month 6 of treatment, the outcome was a healthy male baby. We conclude that intermittent administration of mifepristone can offer a clinically significant improvement of the vaginal bleeding pattern in Norplant users.
AB - A double-blind, placebo-controlled, randomized trial, was carried out in 120 Norplant® users to evaluate the effect of mifepristone, 100 mg/day administered for 2 consecutive days every 30 days, on the vaginal bleeding pattern. Treatment was given from months 2-7 of implant use. Volunteers recorded bleeding and spotting days, during treatment and for the ensuing 6-month period. During treatment, women on mifepristone recorded the same frequency of bleeding/spotting episodes but significantly less prolonged bleeding episodes than placebo controls (mean ± SD: 11 ± 3 vs. 22 ± 23 days) and their total number of bleeding days was 35% lower than in the placebo group. After the end of mifepristone use, bleeding patterns were similar in both groups. One pregnancy occurred in the mifepristone-treated group, in month 6 of treatment, the outcome was a healthy male baby. We conclude that intermittent administration of mifepristone can offer a clinically significant improvement of the vaginal bleeding pattern in Norplant users.
KW - Bleeding
KW - Contraception
KW - Implants
KW - Mifepristone
KW - Progestin-only
UR - http://www.scopus.com/inward/record.url?scp=2942693992&partnerID=8YFLogxK
U2 - 10.1016/j.contraception.2004.02.009
DO - 10.1016/j.contraception.2004.02.009
M3 - Article
C2 - 15208052
AN - SCOPUS:2942693992
SN - 0010-7824
VL - 70
SP - 47
EP - 54
JO - Contraception
JF - Contraception
IS - 1
ER -