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Contraception ; 61(4): 277-80, 2000 Apr.
Article in English | MEDLINE | ID: mdl-10899484

ABSTRACT

A total of 1,904 women, aged 15-38, used an injectable contraceptive combination of 90 mg dihydroxyprogesterone acetophenide with 6 mg estradiol enanthate, given once during each menstrual cycle between the 7th and 10th day, and preferably on the 8th day of the cycle, for a total of 17,576 cycles. Of these 1,904 women, 1,197 completed 12 cycles of use of the injectable combination. One subject became pregnant during the trial, resulting in a cumulative pregnancy rate of 0.07%. Principal reasons for discontinuation were personal, non-medical reasons, such as lost to follow-up, no longer wished to continue, protocol violation, desire to change to another contraceptive method, moved away, or other personal reasons. Mean weight of 1,901 subjects at admission to the trial was 53.5 +/- 0.2 kg and this increased to 54.3 +/- 0.3 kg after 12 cycles of use. Approximately 50% of subjects experienced menstrual bleeding similar to normal throughout the study period. The most frequent menstrual abnormality was irregular bleeding, experienced by approximately one-third of subjects.


Subject(s)
Algestone Acetophenide/administration & dosage , Contraceptive Agents, Female/administration & dosage , Contraceptive Agents, Female/adverse effects , Estradiol/analogs & derivatives , Adolescent , Adult , Double-Blind Method , Estradiol/administration & dosage , Female , Humans , Injections , Menstrual Cycle , Patient Satisfaction , Pregnancy , Uterine Hemorrhage/chemically induced
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