TY - JOUR
T1 - Male hormonal contraception: A double-blind, placebo-controlled study
AU - Mommers, Ellen
AU - Kersemaekers, Wendy M.
AU - Elliesen, Jörg
AU - Kepers, Marc
AU - Apter, Dan
AU - Behre, Hermann M.
AU - Beynon, Jennifer
AU - Bouloux, Pierre M.
AU - Costantino, Antonietta
AU - Gerbershagen, Hans Peter
AU - Grønlund, Lars
AU - Heger-Mahn, Doris
AU - Huhtaniemi, Ilpo
AU - Koldewijn, Evert L.
AU - Lange, Corinna
AU - Lindenberg, Svend
AU - Meriggiola, M. Cristina
AU - Meuleman, Eric
AU - Mulders, Peter F A
AU - Nieschlag, Eberhard
AU - Perheentupa, Antti
AU - Solomon, Andrew
AU - Väisälä, Leena
AU - Wu, Frederick C.
AU - Zitzmann, Michael
N1 - Journal Article United States
PY - 2008/7
Y1 - 2008/7
N2 - Background: This study was performed to assess spermatogenesis suppression and safety of a new combination of an etonogestrel (ENG) implant combined with testosterone undecanoate (TU) injections for male contraception. This is the first large placebo-controlled study for male hormonal contraception. Design and Study Subjects: In this double-blind, multicenter study, we randomly assigned 354 healthy men to receive either a low- or high-release ENG implant sc combined with im TU injections (750 mg every 10 or 12 wk or 1000 mg every 12 wk) or placebo implant and injections. Treatment duration was 42 or 44 wk and posttreatment follow-up at least 24 wk. Results: Overall, spermatogenesis was suppressed to 1 million/ml or less at wk 16 in 89% of men, with approximately 94% in two high-release ENG groups. Suppression was maintained up to the end of the treatment period in 91% of men. For all men who completed the treatment period, 3% never achieved 1 million/ml or less. Median recovery time to a sperm concentration above 20 million/ml was 15 wk (mean 17 wk, 95% confidence interval 16-18 wk). Treatment was well tolerated. As compared with the placebo group, more men in the active treatment groups reported adverse events such as weight gain, mood changes, acne, sweating, or libido change. For both spermatogenesis suppression and safety, differences were small between the active treatment groups. Conclusions: The combination of an ENG implant with TU injections is a well-tolerated male hormonal method, providing effective and reversible suppression of spermatogenesis. Although the results are good, there is still room for improvement, possibly by adjusting the dose regimen or changing the mode of application. Copyright © 2008 by The Endocrine Society.
AB - Background: This study was performed to assess spermatogenesis suppression and safety of a new combination of an etonogestrel (ENG) implant combined with testosterone undecanoate (TU) injections for male contraception. This is the first large placebo-controlled study for male hormonal contraception. Design and Study Subjects: In this double-blind, multicenter study, we randomly assigned 354 healthy men to receive either a low- or high-release ENG implant sc combined with im TU injections (750 mg every 10 or 12 wk or 1000 mg every 12 wk) or placebo implant and injections. Treatment duration was 42 or 44 wk and posttreatment follow-up at least 24 wk. Results: Overall, spermatogenesis was suppressed to 1 million/ml or less at wk 16 in 89% of men, with approximately 94% in two high-release ENG groups. Suppression was maintained up to the end of the treatment period in 91% of men. For all men who completed the treatment period, 3% never achieved 1 million/ml or less. Median recovery time to a sperm concentration above 20 million/ml was 15 wk (mean 17 wk, 95% confidence interval 16-18 wk). Treatment was well tolerated. As compared with the placebo group, more men in the active treatment groups reported adverse events such as weight gain, mood changes, acne, sweating, or libido change. For both spermatogenesis suppression and safety, differences were small between the active treatment groups. Conclusions: The combination of an ENG implant with TU injections is a well-tolerated male hormonal method, providing effective and reversible suppression of spermatogenesis. Although the results are good, there is still room for improvement, possibly by adjusting the dose regimen or changing the mode of application. Copyright © 2008 by The Endocrine Society.
U2 - 10.1210/jc.2008-0265
DO - 10.1210/jc.2008-0265
M3 - Article
SN - 1945-7197
VL - 93
SP - 2572
EP - 2580
JO - Journal of Clinical Endocrinology and Metabolism
JF - Journal of Clinical Endocrinology and Metabolism
IS - 7
ER -