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临床试验/EUCTR2008-003661-19-BE
EUCTR2008-003661-19-BE进行中(未招募)1 期

Invloed van laag gedoseerde hormonale substitutie op insulinespiegels bij postmenopausale vrouwen

niversity Hospital Ghent0 个研究点开始时间: 2009年5月29日最近更新:
相关药物

试验速览

阶段
1 期
状态
进行中(未招募)
发起方

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
Female

入选标准

  • - Postmenopausaal
  • - Leeftijd van 65 jaar of ouder
  • - Nog geen HRT genomen in het verleden of HRT stop en 8 weken wash-out
  • - Bereid tot nemen van lage dosis oestrogenen
  • - Mammografie, maximum 1 jaar geleden
  • - BMI = 25 of BMI > 25
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range

排除标准

  • - Voorgeschiedenis van hormoongevoelige tumoren (bv. borstkanker, endometriumkanker,..)
  • - Contra-indicaties voor hormonale substitutie therapie (bv. CVA, trombosen, …)
  • - Diabetes
  • - Afwijkend klinisch onderzoek bij aanvang van de studie (verdikt endometrium op echo, palpabele borstnodus, ovariële cyste op echo,…).

研究者

发起方
niversity Hospital Ghent

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