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临床试验/NCT00300664
NCT00300664已完成2 期

A Randomized Trial of Human Growth Hormone (hGH) vs Placebo in Intensively Treated Haemato-Oncology Patients.

Royal Marsden NHS Foundation Trust0 个研究点目标入组 150 人开始时间: 2002年7月最近更新:
适应症
相关药物

试验速览

阶段
2 期
状态
已完成
入组人数
150

研究概览

简要总结

About 90% of patients with haemato-oncologic malignancy lose their body muscle mass and also lose weight either due to chemotherapy induced nausea/vomiting or the high catabolic state due to fever, sepsis or chemotherapy. This impacts tremendously on the days in hospital and also on the treatment-related complications. Studies with Human Growth hormone (hGH) have shown that it increases lean body mass in adult patients with AIDS and animal models of cancer. At the same time, in vitro studies have shown that hGH has no effect on tumor cell growth. This study is designed to see if the use of hGH in immunocompromised patients with haematological malignancies prevents the loss of muscle mass and weight loss to some extent.

This will be a blinded 1:1, randomised study including 150 patients whereby the patients will either receive hGH or a placebo. The doctors and the nurses will not know what drug the patient is receiving. Both hGH and the placebo will be given intravenously (if patients are receiving other intravenous antibiotics or haemopoietic support ) or subcutaneously (if platelets are above 20 x 109/L) The treatment will start on the first day of treatment and continue for 6 weeks.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
盲法
Single

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age >= 18 years
  • Patients with haematological malignancies receiving neutropenia (< 0.5 x 109/L) inducing chemotherapy (+/- TBI) requiring hospitalisation.
  • Negative pregnancy test if the patient is of childbearing potential
  • Informed consent

排除标准

  • . Previous treatment with growth hormone 2.Unstable psychiatric conditions
  • Uncontrolled endocrine disorders 4.Chronic severe liver disease: AST or ALT>3x upper limit of normal range
  • Chronic severe renal disease: creatinine>150 µM or repeated positive test for haematuria or proteinuria
  • Severe congestive heart failure
  • Aortic stenosis associated with clinical symptoms eg syncope of angina pectoris
  • Hypertrophic cardiomyopathy
  • Uncontrolled hypertension (diastolic blood-pressure > 105 mm Hg)
  • Diabetes mellitus that is not well controlled with insulin/antidiabetic drugs
  • Severe respiratory disease
  • Known or suspected allergy to growth hormone or any of its constituents
  • History of drug or alcohol abuse within two years prior to study enrolment
  • Exposure to another investigational medication or device currently or within three months prior to enrolment.

研究者

申办方类型
Other

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