跳至主要内容
临床试验/EUCTR2007-007604-15-GB
EUCTR2007-007604-15-GB进行中(未招募)1 期

A Pilot Study of the Effect of Glucocorticoid Receptor Antagonism in Patients with Sub-Clinical Cushing's Syndrome - Glucocorticoid Receptor Antagonism in Sub-Clinical Cushings

Sheffield Teaching Hospitals NHS Foundation Trust0 个研究点目标入组 0 人开始时间: 2008年8月21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)

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

入选标准

  • - male and over 18 years old or postmenopausal women
  • - Patients have adrenal incidentaloma with benign characteristics as assessed on CT or MRI
  • - Patients lack clinical features classically associated with Cushing's Syndrome
  • - Patients have evidence of excess cortisol as shown by lack of supression of serum cortisol using standard routine tests
  • - Patients are on stable antihypertensive and diabetic medication for two months prior to study entry
  • 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

  • Exclusion criteria include:
  • - evidence of local or systemic malignancy
  • - overt Cushing's Syndrome
  • - servere uncontrolled diabetes mellitus or hypertension
  • - pregnancy
  • - clinically significantly impaired cardiovascular function, severe liver disease, significantly impaired renal function
  • - uncontrolled severe active infection
  • - treatment with approved or experimental drugs which work on the adrenal glands
  • - in women a known history of uterine problems
  • - a requirement for steroids for existing disease
  • - impaired mental capacity or markedly abnormal psychiatric evaluation that precludes informed consent

研究者

相似试验

已完成
1 期
Glucocorticoid Receptor Antagonism in Subclinical CushingsSubclinical Cushing's
NCT00721201Sheffield Teaching Hospitals NHS Foundation Trust6
已完成
不适用
A pilot study on prevention of glucocorticoid induced diabetes mellitus by linagliptiPatients scheduled administration of glucocorticoid
JPRN-UMIN000015588Department of Nephrology, Rheumatology, Endocrinology and Metabolism, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences.17
进行中(未招募)
1 期
A study to assess whether a product call relacorilant works and is safe to use in patients with Cushing Syndrome; some patients will receive relacorilant whilst others receive a placebo.Endogenous Cushing syndromeMedDRA version: 20.0 Level: LLT Classification code 10011657 Term: Cushings syndrome System Organ Class: 100000004860
EUCTR2018-003096-35-ESCorcept Therapeutics Incorporated130
进行中(未招募)
1 期
A study to assess whether a product called relacorilant works and is safe to use in patients with Cushing Syndrome; some patients will receive relacorilant whilst others receive a placebo.
EUCTR2018-003096-35-DECorcept Therapeutics Incorporated145
进行中(未招募)
1 期
A study to assess whether relacorilant works and is safe to use in patients with Hypercortisolism due to Cortisol-Secreting Adrenal Adenomas or Hyperplasia; some patients will receive relacorilant whilst others receive a placebo.hypercortisolismMedDRA version: 22.1Level: LLTClassification code 10020611Term: HypercortisolismSystem Organ Class: 100000004860
EUCTR2019-004956-12-ITCORCEPT THERAPEUTICS130