跳至主要内容
临床试验/EUCTR2014-001743-20-ES
EUCTR2014-001743-20-ES进行中(未招募)不适用

A Multicentre, prospective, randomised clinical trial comparing the cost and efficacy of corifolitropina alfa vs Recombinant FSH and / or HP-hMG - Use of the corifolitropina alfa in oocyte donors

IVI Madrid0 个研究点开始时间: 2014年8月14日最近更新:
适应症
相关药物

试验速览

阶段
不适用
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

  • Women aged 18-35 years who meet the entry criteria for the IVI Donor Program and will be receiving stimulation with gonadotropins.
  • - Weight <60 kg
  • - Women with at least 6 antral follicles per ovary
  • - Will to fit the protocol during the study period
  • - Woman who gives written consent to participate in Test
  • 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 300
  • F.1.3 Elderly (>=65 years) no
  • F.1.3.1 Number of subjects for this age range

排除标准

  • - Woman with a basal antral follicle count above 20 or below 6
  • - Women with comorbidities, in the judgment of the investigator, that may interfere with the treatment of ovarian stimulation

研究者

发起方
IVI Madrid

相似试验

进行中(未招募)
不适用
A prospective, randomised, multicenter clinical trial investigating the reduction of Calcineurin inhibitor toxicity by means of steroid free long-term immune suppression with Ciclosporin A and Mycophenolat mofetil in children and adolescents after kidney transplantation - Recaltox-1
EUCTR2007-001166-33-DEniversitaetsklinikum Erlangen-Nuernberg
进行中(未招募)
不适用
A study Protocol for patients with relapsed osteosarcomaHigh malignancy grade of osteosarcoma relapseMedDRA version: 14.1Level: PTClassification code 10031296Term: Osteosarcoma recurrentSystem Organ Class: 10029104 - Neoplasms benign, malignant and unspecified (incl cysts and polyps)
EUCTR2012-001010-42-ITITALIAN SARCOMA GROUP
尚未招募
4 期
Multicentre, prospective, randomised clinical survey to evaluate early fusion rate after instrumented lumbar stabilization with either MectaLIF PEEK lumbar cage or MectaLIF TiPEEK lumbar cageDisorders that are treated with lumbar intervertebral body fusion, such as lumbar spondylolisthesis
JPRN-UMIN000027744INCREASE Co., Ltd.240
尚未招募
4 期
A randomized, controlled, multicentre clinical study of Shengu Capsule in the treatment of postmenopausal osteoporosis (deficiency syndrome of liver and kidney)Postmenopausal Osteoporosis
ITMCTR2100004996Fujian Academy of Chinese Medical Sciences
招募中
1 期
A randomized, controlled, multicentre clinical study of optimizing Yantiao prescription in the treatment of septic shockSeptic shock
ITMCTR2100004495Shuguang Hospital Affiliated to Shanghai University of Chinese Medicine