JPRN-UMIN000003700已完成2 期
Evaluation of the usefulness and safety of goserelin plus tamoxifen as neoadjuvant hormone therapy for premenopausal patients with hormone receptor-positive breast cancer - Evaluation of the usefulness and safety of goserelin plus tamoxifen as neoadjuvant hormone therapy for premenopausal patients with hormone receptor-positive breast cancer
St. Luke's International Hospital0 个研究点目标入组 55 人开始时间: 2010年6月3日最近更新:
适应症
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 发起方
- 入组人数
- 55
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
- ot applicable 至 ot applicable（—）
- 性别
- Female
入选标准
- 未提供
排除标准
- •(1) Patients with previous treatment for the breast cancer. (2) Patients receiving drugs having a potential influence on the status of sex hormones (hormone replacement therapy, raloxifene, etc.). (However, patients after washout for at least 2 months can be enrolled.) (3) Patients with myocardial infarction or congestive heart failure at the past history, or patients who need treatment of ischemic hear disease, arryhythmia or valvular disorder. (4) Patients with active double cancer. (5) Inflammatory breast cancer (6) Synchronous or asynchrous bilateral breast cancer. (7) Allergy for radio-enhancer (8) New test drug (9) Severe psychosomatic disease (10) Patients whom doctors judged inadequate to the enrollment of this study by other reasons.
研究者
相似试验
已完成
不适用
Evaluation of the safety and effectiveness of the MID-C/ApiFix system in adolescent idiopathic scoliosis.Spinal curvature1002837710005944NL-OMON43676Vrije Universiteit Medisch Centrum33
招募中
4 期
A real-world study of the safety and efficacy of Ganmaoling granules (999) in the treatment of the common coldcommon coldITMCTR2000002998China-Japan Friendship Hospital
未知
2 期
A prospective exploratory study on the safety of gastric endoscopic submucosal dissection without cessation of warfarin.The lesion that is indicated in gastric endoscopic submucosal dissection in patients who use warfarin for prevention of thrombosis.JPRN-UMIN000020850The University of Tokyo Hospital Department of Gastroenterology, Graduate School of Medicine15
进行中（未招募）
Unknown
Safety and effectiveness clinical evaluation of the range of injectable medical devices HYDRAGEL C in facial aesthetic treatmentSubjects across groups present with moderate to severe facial aesthetic concerns, including peri-oral lines, nasolabial folds, lip volume deficits, and cheeks/cheekbones volume deficit, as gauged by various dermatological scalesSkin and Connective Tissue DiseasesISRCTN13586698ouna Aesthetics75
进行中（未招募）
不适用
Clinical study to evaluate the safety and effectiveness of the use of two hyaluronic acid injectable products (Perfectha® Derm Lidocaine and Perfectha® Deep Lidocaine) in the treatment of lipsFor Perfectha® Derm Lidocaine: very thin to thin lip volume and with lip contour somewhat well-defined to poorly definedfor Perfectha® Deep Lidocaine: thin to moderate lip volumeISRCTN72858148Sinclair Pharma68