Actively Recruiting

Phase 4
Age: 35Years - 75Years
All Genders
NCT06054035

SGLT2 Inhibition in Addition to Lifestyle Intervention and Risk for Complications in Subtypes of Patients With Prediabetes

Led by University Hospital Tuebingen · Updated on 2025-07-24

170

Participants Needed

9

Research Sites

205 weeks

Total Duration

On this page

Sponsors

U

University Hospital Tuebingen

Lead Sponsor

G

German Federal Ministry of Education and Research

Collaborating Sponsor

AI-Summary

What this Trial Is About

More than 50% of patients with type 2 diabetes develop micro- and/or macrovascular complications during the course of the disease. Additionally, many patients at risk for diabetes develop metabolically driven complications including kidney and heart disease. Thus, it is of utmost importance to improve prevention of T2D and with this complications. Remission of prediabetes, i.e. normalization of hyperglycemia by means of lifestyle intervention is one of the most effective ways to prevent the development of T2D and complications. Novel sub-phenotyping analysis identified clusters of risk for diabetes associated with different complications, opening opportunities to new therapeutic approaches, despite and in addition to lifestyle changes. So far, pharmacological therapy is not indicated for patients with prediabetes. Remission of hyperglycemia associated with prediabetes during lifestyle interventions not only prevents T2D but is also linked with reduced albuminuria and lower microvascular and kidney complications. Thus, reaching normoglycemia (i.e. prediabetes remission) is important for reducing the risk of (pre-)diabetes-associated complications including micro- and even macrovascular disease. In patients with T2D, recent data show that dapagliflozin can improve diabetes remission, and thus, likely complications. However, to date no data have assessed whether or not this is also true in patients with hyperglycemia related to prediabetes which, as outlined above, already causes different complications. Subphenotyping of patients with newly onset diabetes suggests that for some individuals, it would be too late to start interventions against dagainst complications at the time of diagnosis of type 2 diabetes. Therefore, individuals at elevated risk to develop T2D and complications should receive preventive measures well before the diagnosis of T2D. This study will provide evidence whether such an early intervention contributes to the remission of hyperglycemia related to prediabetes to protect from associated complications such as renal disease. The studied population will comprise individuals who have hyperglycemia in the range of prediabetes and are thus prone to not only develop T2D, but also early nephropathy but in clinical practice do not receive medical treatment due to the early stage of the disease. These subjects will receive Dapagliflozin 10 mg or Placebo for 6 months. The placebo treatment arm reflects current practice. In order guarantee a benefit the patients in the placebo arm will receive a lifestyle intervention.

CONDITIONS

Official Title

SGLT2 Inhibition in Addition to Lifestyle Intervention and Risk for Complications in Subtypes of Patients With Prediabetes

Who Can Participate

Age: 35Years - 75Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Male, female or intersexual patients aged between 35 and 75 years (including)
  • Prediabetes defined by fasting glucose 60 100 mg/dL or 2-hour OGTT glucose 60 140 mg/dL
  • Body mass index (BMI) of 20 kg/m2 or higher
  • Thyroid stimulating hormone (TSH) within normal range
  • Ability to understand and follow study instructions
  • Negative pregnancy test for premenopausal women
  • Stable thyroid replacement therapy for at least 3 months before screening if applicable
  • Stable antihypertensive medication including mineralocorticoid receptor antagonists for at least 6 weeks before screening
  • Stable treatment with ACE inhibitors, AT1 receptor antagonists, thiazides, or loop diuretics for at least 2 weeks before screening
  • Understand and voluntarily sign informed consent
  • Investigator agrees participation does not pose unacceptable risk to safety or well-being
Not Eligible

You will not qualify if you...

  • Diagnosed diabetes mellitus
  • Estimated glomerular filtration rate (eGFR) below 60 ml/min/1.73 m2
  • Use of any glucose-altering medications including dapagliflozin or other SGLT2 inhibitors
  • Symptomatic chronic congestive heart disease
  • Recent changes in diuretic or antihypertensive medication (within last 2 weeks or 6 weeks for aldosterone antagonists)
  • Known or suspected orthostatic proteinuria
  • Severe acute or chronic illness including recent cancer, unstable cardiovascular disease, or recent coronary procedures
  • History or current therapy for severe congestive heart failure (NYHA III or IV), pacemaker, or significant aortic stenosis
  • Acute pancreatic disease
  • Rapidly progressing kidney disease or anuria
  • Known HIV infection or positive HIV test
  • History or planned organ transplantation
  • Inflammatory bowel disease or severe gastrointestinal diseases affecting gastric emptying
  • Significant liver disease or elevated liver enzymes beyond specified limits
  • Treatment with glucocorticoids
  • Antibiotic treatment within last 4 weeks
  • History of ketoacidosis
  • Repeated urogenital infections
  • Hemoglobinopathies, hemolytic or chronic anemia with hemoglobin below 12.0 g/dL
  • Psychiatric disorders or recent start of antidepressants or antipsychotics
  • Severe depression screening positive (BDI 60 29)
  • Hypersensitivity to study drug or ingredients
  • Weight loss over 5% in last 3 months
  • Pregnant or breastfeeding women
  • Unwillingness to use effective contraception during and shortly after treatment
  • Current participation in other interventional trials or recent treatment with investigational drugs
  • Previous dapagliflozin or similar therapy within recent five half-lives
  • Unwillingness to be informed about accidental findings
  • Any condition judged by investigator to pose unacceptable risk during study participation

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 9 locations

1

Charité Universitätsmedizin Berlin, Klinik für Endokrinologie und Stoffwechselmedizin

Berlin, Germany

Actively Recruiting

2

Universitätsstudienzentrum für Stoffwechselerkrankungen , Medizinische Klinik und Poliklinik III

Dresden, Germany

Actively Recruiting

3

German Diabetes Center, Leibniz-Center for Diabetes Research at the Heinrich-Heine-University Duesseldorf

Düsseldorf, Germany, 40225

Actively Recruiting

4

Heidelberg University Hospital - Department of Endocrinology and Metabolism

Heidelberg, Germany, 69120

Actively Recruiting

5

Medizinische Klinik und Poliklinik III - Bereich Endokrinologie

Leipzig, Germany

Actively Recruiting

6

Medizinische Klinik I, UKSH Campus LübeckAG Meyhöfer - Endocrinology, Diabetes & Metabolism

Lübeck, Germany, 23562

Not Yet Recruiting

7

Diabetes Center Med. Klinik und Poliklinik IV, Klinikum der Universität München, LMU

München, Germany

Actively Recruiting

8

Institut für Ernährungsmedizin, Technische Universität München

München, Germany

Not Yet Recruiting

9

University Hospital Tuebingen, Otfried-Mueller Str. 10

Tübingen, Germany, 72076

Actively Recruiting

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Research Team

A

Andreas Birkenfeld, Prof. Dr.

CONTACT

A

Andreas Fritsche, Prof. Dr.

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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