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1.
Contraception ; 85(5): 480-8, 2012 May.
Artículo en Inglés | MEDLINE | ID: mdl-22176795

RESUMEN

BACKGROUND: Progesterone receptor modulators (PRMs) delivered by contraceptive vaginal rings provide an opportunity for development of an estrogen-free contraceptive that does not require daily oral intake of steroids. The objective of this proof-of-concept study was to determine whether continuous delivery of 600-800 mcg of ulipristal acetate (UPA) from a contraceptive vaginal ring could achieve 80% to 90% inhibition of ovulation. STUDY DESIGN: This was a prospective, controlled, open-labeled, multicenter international trial to examine the effectiveness and safety of this prototype vaginal ring. Thirty-nine healthy women, 21-40 years old and not at risk of pregnancy, were enrolled at three clinic sites. Volunteers participated in a control cycle, a 12-week treatment period and a post-treatment cycle. Pharmacodynamic effects on follicular function and inhibition of ovulation, effects on endometrium, bleeding patterns and serum UPA levels were evaluated. RESULTS: Mean UPA levels during treatment were nearly constant, approximately 5.1 ng/mL throughout the study. Ovulation was documented in 32% of 111 "4-week treatment cycles." A correlation was observed between serum UPA and degree of inhibition of ovarian activity. There was no evidence of hyperplasia of endometrium, but PRM-associated endometrial changes were frequently observed (41%). CONCLUSION: In this study, the minimum effective contraceptive dose was not established. Further studies are required testing higher doses of UPA to attain ovulation suppression in a higher percentage of subjects.


Asunto(s)
Anticonceptivos Femeninos/farmacología , Dispositivos Anticonceptivos Femeninos , Endometrio/efectos de los fármacos , Menstruación/efectos de los fármacos , Norpregnadienos/farmacología , Inhibición de la Ovulación/efectos de los fármacos , Receptores de Progesterona/antagonistas & inhibidores , Adulto , Biomarcadores/metabolismo , Proliferación Celular/efectos de los fármacos , Anticonceptivos Femeninos/administración & dosificación , Anticonceptivos Femeninos/efectos adversos , Anticonceptivos Femeninos/farmacocinética , Dispositivos Anticonceptivos Femeninos/efectos adversos , Preparaciones de Acción Retardada/administración & dosificación , Preparaciones de Acción Retardada/efectos adversos , Preparaciones de Acción Retardada/farmacocinética , Preparaciones de Acción Retardada/farmacología , Endometrio/citología , Endometrio/metabolismo , Femenino , Antagonistas de Hormonas/administración & dosificación , Antagonistas de Hormonas/efectos adversos , Antagonistas de Hormonas/farmacocinética , Antagonistas de Hormonas/farmacología , Humanos , Inmunohistoquímica , Menstruación/sangre , Menstruación/metabolismo , Norpregnadienos/administración & dosificación , Norpregnadienos/efectos adversos , Norpregnadienos/farmacocinética , Folículo Ovárico/efectos de los fármacos , Adulto Joven
2.
Ginecol Obstet Mex ; 72: 76-84, 2004 Feb.
Artículo en Español | MEDLINE | ID: mdl-15216905

RESUMEN

Although classically the antiprogestins have been used for the control of pregnancy diseases and adrenal function, in the medical literature are a plenty of papers about the treatment with progesterone antagonists of leiomyoma, breast cancer, endometriosis and meningioma. The treatment is beneficial or mitigating in greatest number of cases, but they have other different uses than usual like contraception and abortion.


Asunto(s)
Antagonistas de Hormonas , Mifepristona , Progesterona/antagonistas & inhibidores , Ensayos Clínicos como Asunto , Femenino , Antagonistas de Hormonas/farmacocinética , Antagonistas de Hormonas/farmacología , Antagonistas de Hormonas/uso terapéutico , Humanos , Mifepristona/farmacocinética , Mifepristona/farmacología , Mifepristona/uso terapéutico
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