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A Randomized, Controlled Trial of Levonorgestrel Vs. The Yuzpe Regimen as Emergency Contraception Method among Iranian Women.
Hoseini, Fatemeh Sadat; Eslami, Mohammad; Abbasi, Mohammed; Noroozi Fashkhami, Fatemeh; Besharati, Soheila.
Afiliação
  • Hoseini FS; 1. Dept. of Anatomy, School of Medicine, Tehran University of Medical Sciences , Tehran, Iran.
  • Eslami M; 2. Dept. of Population, Family and School Health, Ministry of Health and Medical Education , Tehran, Iran.
  • Abbasi M; 3. Family Planning Office, Gilan University of Medical Sciences , Rasht, Iran.
  • Noroozi Fashkhami F; 3. Family Planning Office, Gilan University of Medical Sciences , Rasht, Iran.
  • Besharati S; 3. Family Planning Office, Gilan University of Medical Sciences , Rasht, Iran.
Iran J Public Health ; 42(10): 1158-66, 2013 Oct.
Article em En | MEDLINE | ID: mdl-26060625
BACKGROUND: We aimed to compare acceptability of Levonorgestrel with the Yuzpe regimen among Iranian women based on their side-effects and resulting changes in the amount and pattern of menses. METHODS: Five hundred twenty nine participants aged 15-49 having regular menses and one act of unprotected intercourse within 72 h were included in the double-blind, controlled trial in 2006-2007 and randomly assigned into LNG (n=263) and HD (n=266) groups, receiving Levonorgestrel 0.75 mg given 12 h apart and ethinyl estradiol 100 µg plus 0.5 mg Levonorgestrel 0.5 mg repeated after 12 h, respectively. RESULTS: The participants receiving Levonorgestrel experienced significantly lower side-effects in the case of nausea, vomiting, and dizziness (P<0.05). The changes occurred in the amount and pattern of menses were the same for both groups (P>0.05). No significant difference was observed between the efficiencies of the treatments. CONCLUSION: Significantly lower side-effects of Levonorgestrel can be considered as greater acceptability and translated to higher efficiency.
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Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Clinical_trials Idioma: En Ano de publicação: 2013 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Clinical_trials Idioma: En Ano de publicação: 2013 Tipo de documento: Article