Improved therapeutic management of women with endometriosis
This study compared dienogest alone versus dienogest combined with mebicar and phenibutum for endometriosis, finding the combination therapy slightly more effective over six months.
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The paper reports development and testing of a complex drug therapy regimen in 80 women with endometriosis, including 80 women with adenomyosis, divided into two groups and followed for six months. In group 1 (n=42), participants received dienogest (Vissane) 2 mg daily for six months, while group 2 (n=38) received dienogest 2 mg daily for six months plus mebicar (Adaptol) 500 mg twice daily and phenibut (Noophen) 250 mg twice daily for three months. The authors found slightly higher clinical efficacy for the combined therapy with non-hormonal drugs compared with progestin therapy alone. This paper is centrally about endometriosis — it evaluates improved therapeutic management using dienogest alone versus dienogest combined with Adaptol and Noophen, with adenomyosis included in the study population.
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Cites (3)
- Dienogest is a selective progesterone receptor agonist in transactivation analysis with potent oral endometrial activity due to its efficient pharmacokinetic profile 2007
- The inhibitory effect of dienogest, a synthetic steroid, on the growth of human endometrial stromal cells in vitro 2001
- Dienogest, a synthetic progestin, inhibits the proliferation of immortalized human endometrial epithelial cells with suppression of cyclin D1 gene expression 2009
Cited by (1)
References (5)
- Dienogest, a synthetic progestin, inhibits the proliferation of immortalized human endometrial epithelial cells with suppression of cyclin D1 gene expression via openalex
- Dienogest is a selective progesterone receptor agonist in transactivation analysis with potent oral endometrial activity due to its efficient pharmacokinetic profile via openalex
- The inhibitory effect of dienogest, a synthetic steroid, on the growth of human endometrial stromal cells in vitro via openalex
- W1965699572 via openalex
- W2096141938 via openalex
Cited by (1)
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- openalex
- last seen: 2026-06-10T17:14:06.276822+00:00