Skip to main content
OpenTrials
Completed

NCT Number: NCT03814915

Diabetes Research on Patient Stratification

The overarching goal of the IMI DIRECT (Innovative Medicines Initiative Diabetes Research on Patient Stratification) Consortium is the identification of biomarkers that aid therapeutic targeting in prediabetes (Study 1) or early onset type 2 diabetes (Study 2).

Completed

Looking for future studies?

Notify Me

Key information

About this study

There are two multicentre prospective cohort studies within the glycaemic deterioration work package of IMI DIRECT (WP2). These two cohorts are designed to address the area of glycaemic deterioration by amassing data and biomaterials that will be used to discover novel biomarkers for glycaemic deterioration in people at high risk of developing type 2 diabetes (Study 1) and in those who have recently been diagnosed with the disease (Study 2).

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Study 1

Inclusion criteria

  • No treatment with insulin-sensitising, glucose-lowering or other antidiabetic drugs
  • Fasting capillary blood glucose <10 mmol/l at baseline
  • White European (self-report of parental ethnicity)
  • Age ≥35 and <75 years

Exclusion criteria

  • Diagnosed diabetes of any type, HbA1c ≥6.5% (48 mmol/mol) or fasting plasma glucose ≥7.0 mmol/l or 2 h plasma glucose >11.0 mmol/l previously
  • For women, pregnancy, lactation or plans to conceive within the study period
  • Use of a pacemaker
  • Any other significant medical reason for exclusion as determined by the investigator

Study 2

Inclusion criteria

  • Patients diagnosed with type 2 diabetes not less than 6 months and not more than 24 months before baseline examination
  • Management by lifestyle with or without metformin therapy
  • All HbA1c <7.6% (<60 mmol/mol) within previous 3 months
  • White European
  • Age ≥35 and <75
  • Estimated GFR >50 ml/min'

Exclusion criteria

  • Type 1 diabetes
  • A previous HbA1c >9.0% (>75 mmol/mol)
  • Prior treatment with insulin or an oral hypoglycaemic agent other than metformin
  • BMI <20 or >50 kg/m2
  • Pregnancy, lactation or plans to conceive within the study period
  • Any other significant medical reason for exclusion as determined by the investigator

Treatment and study plan

Primary outcomes

  1. Glycemic deterioration

    Time frame: Up to 10 years follow-up

    Change in glucose (or HbA1c) over time and/or progression to anti diabetic medications/insulin

Sponsors and collaborators

Lead sponsor

Lund University

Other

Registry information

Acronym: DIRECT

Important dates

Study start
2012
Primary completion
2019
Study completion
2019
First posted
Jan 24, 2019
Registry last updated
Jan 18, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.