跳至主要内容
临床试验/ISRCTN88646091
ISRCTN88646091进行中(未招募)4 期

Diabetes Interventional Assessment of Slimming or Training tO Lessen Inconspicuous Cardiovascular dysfunction (DIASTOLIC)

niversity of Leicester0 个研究点目标入组 120 人开始时间: 2015年11月25日最近更新:
适应症

试验速览

阶段
4 期
状态
进行中(未招募)
发起方
入组人数
120

研究概览

简要总结

  1. 2018 preliminary study in: https://www.ncbi.nlm.nih.gov/pubmed/29661781 (added 10/04/2019) 2. 2019 protocol in: https://www.ncbi.nlm.nih.gov/pubmed/30928925 (added 10/04/2019)

研究设计

研究类型
Interventional

入排标准

性别
All

入选标准

  • Diabetic patient inclusion criteria:
  • 1. Aged between 18 and 60 years
  • 2. Capacity to provide informed consent before any trial­ related activities
  • 3. Established T2DM for at least 3 months
  • 4. HbA1c = 9% if on triple therapy or = 10% on diet & exercise or monotherapy or dual therapy
  • 5. Current glucose lowering therapy either mono, dual or triple of any combination of metformin, sulphonylurea, DPP­IV inhibitor, GLP­1 therapy or an SGLT2 +/-­ diet and exercise
  • 6. Body mass index > 30Kg/m2 (white Europeans) or > 27Kg/m2 (South East Asian or Afro-­Caribbean)
  • 7. Diagnosis of T2DM before the age of 50 years of age
  • Healthy controls inclusion criteria:
  • 1. Aged between 18 and 60 years
  • 2. Capacity to provide informed consent before any trial­ related activities
  • 3. Body mass index < 30Kg/m2 (white Europeans) or < 27Kg/m2 (South East Asian or Afro-­Caribbean)
  • 4. No cardiovascular symptoms (angina, limiting dyspnoea)

排除标准

  • Diabetic patient exclusion criteria:
  • 1. Aged under 18 or over 60
  • 2. HbA1c >10%
  • 3. Diabetes duration >12 years
  • 4. Currently taking more than three glucose lowering therapies
  • 5. Weight-loss of >5kg in the preceding 6 months
  • 6. Stage 4 or 5 chronic kidney disease (eGFR <30ml/min/1.73m2)
  • 7. Current therapy with insulin, thiazolidinediones (or within the preceeding three months), steroids or atypical antipsychotic medication, untreated thyroid disease
  • 8. Known ischaemic heart disease or heart failure
  • 9. Inability to exercise or undertake a TDR
  • 10. Absolute contraindication to CMR
  • 11. Cardiovascular symptoms (angina, limiting dyspnoea).
  • 12. Patients with asthma will be assessed for suitability of adenosine stress. If adenosine is contraindicated (severe asthma) subjects can participate without perfusion assessment
  • 13. Inflammatory condition e.g. connective tissue disorder, rhematoid arthritis.
  • Healthy controls inclusion criteria:
  • 1. Aged under 18 or over 60
  • 2. Diabetes or impaired glucose tolerance
  • 3. Obesity (BMI >30 (white european) or >27 (Asian or Afro-Caribbean)
  • 4. Severe asthma
  • 5. History of hypertension, or blood pressure in excess of either 160mmHG systolic or 100mmHG diastolic and currently untreated
  • 6. Inflammatory condition e.g. connective tissue disorder, rheumatoid arthritis
  • 7. Congenital heart disease
  • 8. Renal impairment (eGFR <60ml/min/m2)
  • 9. Other conditions that in the opinion of the investigators may limit exercise capacity or be associated with subclinical cardiac dysfunction
  • 10. Competitive athletes

研究者

发起方
niversity of Leicester

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