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临床试验/EUCTR2016-004772-21-IT
EUCTR2016-004772-21-IT进行中(未招募)1 期

Dual-release hydrocortisone compared to immediate-release glucocorticoid replacement therapy in terms of glucose control, insulin sensitivity and glucose variability in patients with adrenal insufficiency and concomitant diabetes mellitus. - Dual-release hydrocortisone compared to immediate-release glucocorticoid replacement therapy in pati

AZIENDA OSPEDALIERA UNIVERSITARIA INTEGRATA VERONA0 个研究点目标入组 16 人开始时间: 2021年6月8日最近更新:
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试验速览

阶段
1 期
状态
进行中(未招募)
入组人数
16

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
All

入选标准

  • The inclusion criteria for the participants in this study are as follows:
  • Males and females older than 18 years up to 90 years of age (women of childbearing age they will perform a high sensitivity pregnancy test to exclude a pregnancy before being included in the study);
  • diagnosis of primitive or secondary adrenal insufficiency;
  • Stable substitution treatment (same dosage and same active principle) with glucorticoids for at least 6 months;
  • - Substitution treatment with L-thyroxin and / or fludrocortisone stable at least 3 months before
  • Concomitant diagnosis of DMT1 or DMT2, in multiinjection insulin therapy or with Oral hypoglycemic agents.
  • Affected at the Hospitals' Diabetes / Endocrinology Outpatient Clinic University of Verona;
  • optimization of metabolic control prior to entry into the study in the presence of clinically stable HbA1c values ¿¿(variations of less than 0.3%) in the two controls prior to recruitment, spaced at least 3 months apart;
  • Signature of informed consent
  • 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 8
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 8

排除标准

  • Subjects will be excluded from the study with the following characteristics:
  • - Pregnant women or fertile age in extroprogestine therapy for contractual purposes;
  • - breastfeeding women;
  • - subjects with hypersensitivity to the active substance or to any of the excipients
  • - Gastrointestinal motility disorders;
  • - Adrenal insufficiency secondary to the suspension of chronic steroid treatment;
  • Cortical-adrenal carcinoma
  • - Coexistence of other pathologies that may require a treatment cycle high doses of steroids.

研究者

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