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临床试验/PER-040-03
PER-040-03已完成1 期

INTERNATIONAL MULTICENTRIC STUDY OF TAMOXIFEN VS. ANASTROZOL IN WOMEN POST-MENOPAUSICAS WITH CARCINOMA DUCTAL IN SITU IBIS II (DCIS).

ASTRAZENECA - PERU,0 个研究点目标入组 0 人开始时间: 2003年8月6日最近更新:
适应症

试验速览

阶段
1 期
状态
已完成
发起方

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
0 至 0(—)

入选标准

  • a) All women must be post-menopausal and have between 40 to
  • 70 years. The post-menopausal state is defined as 1 or more of
  • the following criteria: Greater than 60 years, bilateral Ortectomy, less than 60 years with uterus and amenorrhea of at least 12 months, less than 60 years without uterus and with FSH> 20 Ul / L.
  • b) CDIS locally resected within the last 6 months.
  • c) Having baseline bone densitometry within the last 2 years will be required in all women. A column radiograph to rule out
  • Frailty fractures will also be required.

排除标准

  • a) Pre-menopausal woman.
  • b) Any previous cancer in the last 5 years (except non-melanoma skin cancer or in situ cancer of the cervix).
  • c) Current treatment with anticoagulants.
  • d) Deep vein thrombosis or previous puimonar embolism.
  • e) Transient ischemic cerebral accident (TIA) or previous cerebrovascular accident.
  • f) Current or previous administration of Tamoxifen or Raloxifene or other SERMs for more than 3 months or participation in IBIS-I.
  • g) Intention to continue with the use of hormone replacement therapy
  • based on estrogens.
  • h) Women who have had a prophylactic mastectomy or are planning to perform this procedure.
  • i) Any woman with post-menopausal bleeding not explained.

研究者

发起方
ASTRAZENECA - PERU,

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