- ICH GCP
- Registro degli studi clinici negli Stati Uniti
- Sperimentazione clinica NCT02015299
Off taRget Effects of Linagliptin monothErapy on Arterial Stiffness in Early Diabetes (RELEASE)
Diabetes is associated with an increased risk for developing premature macrovascular complications. The process of irreversible subclinical damage to the vasculature already starts during its preceding stages. Dipeptidyl peptidase (DPP)-4 inhibitors have been shown to attenuate vascular damage in preclinical studies. Off-target effects on adipose tissue inflammation, liver steatosis and atherosclerotic plaques have been extensively documented in animal studies.
Based on these considerations the investigators hypothesize that early therapy with the DPP4 inhibitor linagliptin in subjects with treatment naive type 2 diabetes will lead to beneficial effects on arterial stiffness as measured by pulse wave velocity.
Panoramica dello studio
Stato
Condizioni
Intervento / Trattamento
Descrizione dettagliata
Tipo di studio
Iscrizione (Effettivo)
Fase
- Fase 3
Contatti e Sedi
Luoghi di studio
-
-
-
Groningen, Olanda, 9700 RB
- University Medical Center Groningen
-
-
Criteri di partecipazione
Criteri di ammissibilità
Età idonea allo studio
Accetta volontari sani
Sessi ammissibili allo studio
Descrizione
Inclusion Criteria:
- Men and women, age 30 to 70 years, AND
- Treatment naïve type 2 diabetes, as defined as t
- Fasting plasma glucose ≥ 7.0 mmol/l, OR
- Random plasma glucose ≥ 11.1 mmol/l, OR
- HbA1c ≥6,5%
- Written informed consent
- Assessable Pulse Wave Velocity measurement at screening
Exclusion Criteria:
- Current or previous use of glycemic control medications
- Type 1 diabetes
- Gestational diabetes mellitus
- Other specific types of diabetes due to other causes, e.g., genetic defects in β-cell function, genetic defects in insulin action, diseases of the exocrine pancreas (such as cystic fibrosis), and drug- or chemical-induced (such as in the treatment of HIV/AIDS or after organ transplantation)
- Uncontrolled hypertension, defined as systolic blood pressure >160 or a diastolic blood pressure >100 mmHg at screening visit
- Severe dyslipidemia indicating primary dyslipidemia, defined as total cholesterol >8 mmol/l, triglycerides >10 mmol/l of high density lipoprotein cholesterol <0.6 mmol/l
- Current use of weight loss medication or previous weight loss surgery
- History of severe gastrointestinal disease
- Clinical contraindications to DPP4-inhibitors
- Previous cardiovascular disease, defined as stable coronary artery disease or acute coronary syndrome, stroke or transient ischemic attack, peripheral artery disease
- Symptomatic heart failure, New York Heart Association (NYHA) class II-IV
- Women who are currently pregnant,planning to become pregnant,breastfeeding women, or women with child bearing potential not using appropriate contraceptive measures
- Clinically significant liver disease or hepatic function greater than 3 times upper limit of normal
- Known impaired renal function or eGFR <30 ml/min/1.73m2
- Patients who are mentally incompetent and cannot sign a Patient Informed Consent
- Current active malignancy or in the previous 6 months
- Documented HIV infection
- Use of rifampicin
Piano di studio
Come è strutturato lo studio?
Dettagli di progettazione
- Scopo principale: Trattamento
- Assegnazione: Randomizzato
- Modello interventistico: Assegnazione parallela
- Mascheramento: Quadruplicare
Armi e interventi
Gruppo di partecipanti / Arm |
Intervento / Trattamento |
|---|---|
|
Sperimentale: Linagliptin
Linagliptin 5 mg/day + lifestyle advise
|
one tablet linagliptin 5 mg/day for 26 weeks
Altri nomi:
|
|
Comparatore placebo: Placebo
Matching placebo + lifestyle advise
|
one tablet matching placebo/day for 26 weeks
|
Cosa sta misurando lo studio?
Misure di risultato primarie
Misura del risultato |
Lasso di tempo |
|---|---|
|
change from baseline carotid-(right) femoral arterial Pulse Wave Velocity (PWV) at 26 weeks
Lasso di tempo: baseline, week 26
|
baseline, week 26
|
Misure di risultato secondarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
|
Secondary vascular study parameters
Lasso di tempo: baseline, week 4, week 26, and 4 weeks after treatment discontinuation (week 30)
|
|
baseline, week 4, week 26, and 4 weeks after treatment discontinuation (week 30)
|
|
Subclinical vascular inflammation (FDG PET-CT)
Lasso di tempo: 26 weeks
|
Target-to-background ratios (TBRs) (18)F-fluorodeoxyglucose positron emission tomography computed tomography coregistration (FDG PET-CT)
|
26 weeks
|
Altre misure di risultato
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
|
Body Mass Index and Waist-to-Hip ratio
Lasso di tempo: baseline, week 4, week 26, and 4 weeks after treatment discontinuation (week 30)
|
Body Mass Index and Waist-to-Hip ratio
|
baseline, week 4, week 26, and 4 weeks after treatment discontinuation (week 30)
|
|
Blood pressure
Lasso di tempo: baseline, week 4, week 26, and 4 weeks after treatment discontinuation (week 30)
|
24-hours ambulatory blood pressure measurement (24-ABPM)
|
baseline, week 4, week 26, and 4 weeks after treatment discontinuation (week 30)
|
|
Advanced glycation end products
Lasso di tempo: baseline, week 4, week 26, and 4 weeks after treatment discontinuation (week 30)
|
Skin AGE deposition measured and plasma levels of AGEs
|
baseline, week 4, week 26, and 4 weeks after treatment discontinuation (week 30)
|
|
plasma markers of inflammation
Lasso di tempo: baseline, week 26
|
baseline, week 26
|
|
|
plasma markers of endothelial dysfunction
Lasso di tempo: baseline, week 26
|
baseline, week 26
|
|
|
Glycemic indices
Lasso di tempo: baseline, week 4, week 26, and 4 weeks after treatment discontinuation (week 30)
|
Fasting glucose (FPG) and 2-hour post OGTT glucose (OGTT), HbA1c
|
baseline, week 4, week 26, and 4 weeks after treatment discontinuation (week 30)
|
|
albuminuria
Lasso di tempo: baseline, week 4, week 26, and 4 weeks after treatment discontinuation (week 30)
|
Urinary albumin/creatinine ratio
|
baseline, week 4, week 26, and 4 weeks after treatment discontinuation (week 30)
|
|
Lifestyle
Lasso di tempo: baseline, week 26
|
Intake of energy, Eating behaviour, and Physical activity
|
baseline, week 26
|
Collaboratori e investigatori
Sponsor
Collaboratori
Investigatori
- Investigatore principale: Pieter W Kamphuisen, MD PhD, University Medical Center Groningen
Pubblicazioni e link utili
Pubblicazioni generali
- Reijrink M, de Boer SA, Spoor DS, Lefrandt JD, Lambers Heerspink HJ, Boellaard R, Greuter MJ, Borra RJH, Hillebrands JL, Slart RHJA, Mulder DJ. Visceral adipose tissue volume is associated with premature atherosclerosis in early type 2 diabetes mellitus independent of traditional risk factors. Atherosclerosis. 2019 Nov;290:87-93. doi: 10.1016/j.atherosclerosis.2019.09.016. Epub 2019 Sep 25.
- de Boer SA, Hovinga-de Boer MC, Heerspink HJ, Lefrandt JD, van Roon AM, Lutgers HL, Glaudemans AW, Kamphuisen PW, Slart RH, Mulder DJ. Arterial Stiffness Is Positively Associated With 18F-fluorodeoxyglucose Positron Emission Tomography-Assessed Subclinical Vascular Inflammation in People With Early Type 2 Diabetes. Diabetes Care. 2016 Aug;39(8):1440-7. doi: 10.2337/dc16-0327. Epub 2016 Jun 8.
Studiare le date dei record
Studia le date principali
Inizio studio
Completamento primario (Effettivo)
Completamento dello studio (Effettivo)
Date di iscrizione allo studio
Primo inviato
Primo inviato che soddisfa i criteri di controllo qualità
Primo Inserito (Stima)
Aggiornamenti dei record di studio
Ultimo aggiornamento pubblicato (Stima)
Ultimo aggiornamento inviato che soddisfa i criteri QC
Ultimo verificato
Maggiori informazioni
Termini relativi a questo studio
Parole chiave
Termini MeSH pertinenti aggiuntivi
- Disturbi del metabolismo del glucosio
- Malattie metaboliche
- Malattie del sistema endocrino
- Diabete mellito
- Diabete mellito, tipo 2
- Agenti ipoglicemizzanti
- Effetti fisiologici delle droghe
- Meccanismi molecolari dell'azione farmacologica
- Inibitori enzimatici
- Ormoni
- Ormoni, sostituti ormonali e antagonisti ormonali
- Inibitori della proteasi
- Incretine
- Linagliptin
- Inibitori della dipeptidil-peptidasi IV
Altri numeri di identificazione dello studio
- NL43473.042.13
Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .
Prove cliniche su Linagliptin
-
Yanbing LiNon ancora reclutamento
-
Boehringer IngelheimEli Lilly and CompanyCompletatoDiabete mellito, tipo 2Cina, Malaysia, Filippine, Vietnam
-
Genuine Research Center, EgyptEva PharmaCompletato
-
Evidem Consultores SLBoehringer Ingelheim; Merck Serono International SA; European CommissionSconosciuto
-
Boehringer IngelheimCompletatoDiabete mellito, tipo 2Canada, Croazia, Estonia, Francia, Germania, India, Lituania, Messico, Olanda, Romania, Federazione Russa, Svezia, Tunisia, Ucraina
-
JW PharmaceuticalReclutamentoDiabete mellito di tipo 2 (T2DM)Corea del Sud
-
Boryung Pharmaceutical Co., LtdCompletatoIpertensione | DiabeteCorea, Repubblica di
-
Boehringer IngelheimEli Lilly and CompanyCompletatoDiabete mellito, tipo 2Bangladesh, Belgio, Canada, Cina, Germania, Guatemala, Hong Kong, India, Libano, Messico, Perù, Filippine, Spagna, Taiwan
-
Boehringer IngelheimCompletato