Abstract | OBJECTIVE: METHODS: 56 women, aged 22 to 50, affected by menstrual disorders or premenstrual syndrome, entered the study. They were divided in two homogeneous groups by randomization. In the first group nomegestrol acetate was administered 5 mg daily per os; in the second group patients were treated by the usual didrogesteron dose, that is 10 mg twice a day per os; both treatments were administered for 10 days from day 16, during three consecutive menstrual cycles. Efficacy, compliance and biological tolerance were evaluated. RESULTS: 24 patients in the group treated by nomegestrol acetate and 22 in the group treated by didrogesteron completed the study. After the first cycle of therapy, nomegestrol acetate showed a higher efficacy in reducing menstrual loss; results are statistically homogeneous in the two groups at the end of the study. There were no reports of pain in both the groups. Evaluation of biological and clinical parameters at the end of the study did not show significant modifications in any subject. CONCLUSIONS:
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Authors | P Persiani, E Radici, P A Lombardi, P L Lombardi |
Journal | Minerva ginecologica
(Minerva Ginecol)
Vol. 49
Issue 4
Pg. 181-5
(Apr 1997)
ISSN: 0026-4784 [Print] Italy |
Vernacular Title | Utilizzo del nomegestrolo acetato nella terapia delle irregolarità mestruali. Esperienza di 56 casi. |
PMID | 9206771
(Publication Type: Clinical Trial, Comparative Study, English Abstract, Journal Article, Randomized Controlled Trial)
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Chemical References |
- Norpregnadienes
- Progesterone Congeners
- Progesterone
- nomegestrol acetate
- Megestrol
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Topics |
- Adult
- Amenorrhea
(drug therapy)
- Female
- Humans
- Megestrol
- Menstrual Cycle
- Menstruation Disturbances
(drug therapy)
- Norpregnadienes
(therapeutic use)
- Oligomenorrhea
(drug therapy)
- Premenstrual Syndrome
(drug therapy)
- Progesterone
(analogs & derivatives, therapeutic use)
- Progesterone Congeners
(therapeutic use)
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