SGLT2 Inhibition in Addition to Lifestyle Intervention and Risk for Complications in Subtypes of Patients With Prediabetes - a Randomized, Placebo Controlled, Multi-center Trial

Status: Recruiting
Location: See all (9) locations...
Intervention Type: Behavioral, Drug
Study Type: Interventional
Study Phase: Phase 4
SUMMARY

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.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 35
Maximum Age: 75
Healthy Volunteers: f
View:

• Male, female or intersexualpatients aged between 35 and 75 years (including)

• Prediabetes (defined by one of the following: FG ≥ 100 mg/dL or 2h OGTT glucose ≥ 140 mg/dL)

• BMI ≥20 kg/m2

• TSH within normal range

• Ability to understand and follow study-related instructions

• Negative pregnancy test for premenopausal women (blood)

• Patients who are receiving thyroid replacement therapy must be on a stable treatment regimen for at least 3 months prior to the screening visit (V-1)

• Patients who are receiving antihypertensive medication such as mineralocorticoid receptor antagonists must be on a stable treatment regimen for at least 6 weeks prior to the screening visit (V-1)

• Patients who are treated antihypertensive medication such as ACE inhibitors and AT1receptor antagonists, thiazides as well as loop diuretics must be on stable treatment for at least 2 weeks

⁃ Understand and voluntarily sign an informed consent document prior to any study related assessments/procedures.

⁃ Patients will not be included in the study if, in the opinion of the investigator participation will lead to an unacceptable risk to the subjects' safety or well-being

Locations
Other Locations
Germany
Charité Universitätsmedizin Berlin, Klinik für Endokrinologie und Stoffwechselmedizin
RECRUITING
Berlin
Universitätsstudienzentrum für Stoffwechselerkrankungen , Medizinische Klinik und Poliklinik III
RECRUITING
Dresden
German Diabetes Center, Leibniz-Center for Diabetes Research at the Heinrich-Heine-University Duesseldorf
RECRUITING
Düsseldorf
Heidelberg University Hospital - Department of Endocrinology and Metabolism
RECRUITING
Heidelberg
Medizinische Klinik und Poliklinik III - Bereich Endokrinologie
RECRUITING
Leipzig
Medizinische Klinik I, UKSH Campus LübeckAG Meyhöfer - Endocrinology, Diabetes & Metabolism
NOT_YET_RECRUITING
Lübeck
Diabetes Center Med. Klinik und Poliklinik IV, Klinikum der Universität München, LMU
RECRUITING
München
Institut für Ernährungsmedizin, Technische Universität München
NOT_YET_RECRUITING
München
University Hospital Tuebingen, Otfried-Mueller Str. 10
RECRUITING
Tübingen
Contact Information
Primary
Andreas Birkenfeld, Prof. Dr.
andreas.birkenfeld@med.uni-tuebingen.de
0049707129
Backup
Andreas Fritsche, Prof. Dr.
andreas.fritsche@med.uni-tuebingen.de
0049707129
Time Frame
Start Date: 2023-10-26
Estimated Completion Date: 2027-09-30
Participants
Target number of participants: 170
Treatments
Experimental: Dapagliflozin (Forxiga®) and lifestyle counselling
Placebo_comparator: Placebo matching Dapaglifolzin and lifestyle counselling
Related Therapeutic Areas
Sponsors
Leads: University Hospital Tuebingen
Collaborators: AstraZeneca, German Center for Diabetes Research, German Federal Ministry of Education and Research

This content was sourced from clinicaltrials.gov