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Renal Insufficiency And Cardiovascular Events (RIACE)

9. februar 2015 opdateret af: Giuseppe Pugliese, Diabetic Nephropathy Study Group

Reduced Estimated Glomerular Filtration Rate (eGFR)and Prediction of Cardiovascular Disease and Renal Outcome in Subjects With Type 2 Diabetes: Italian Multicenter Study

Reduced glomerular filtration rate (GFR) has been recently shown to be a powerful predictor of cardiovascular morbidity and mortality in the general population, independent of traditional cardiovascular risk factors.

This observational study is aimed at assessing the association of reduced estimated GFR with cardiovascular morbidity and mortality in a large italian population (at least 15,000 subjects) of type 2 diabetic outpatients over a 4-year follow-up.

Studieoversigt

Status

Afsluttet

Detaljeret beskrivelse

Reduced GFR has been recently shown to be a powerful predictor of cardiovascular morbidity and mortality in the general population, independent of traditional cardiovascular risk factors. Since type 2 diabetic patients show increased cardiovascular morbidity and mortality as compared with the general population, the identification of predictors of cardiovascular disease in these patients is of fundamental importance for clinical purposes. One of these predictors is increased urinary albumin excretion rate, which is associated with an increased risk of cardiovascular disease more than of end-stage renal disease. However, a growing body of evidence indicates that a significant proportion of normoalbuminuric diabetic patients, particularly with type 2 diabetes, may exhibit reduced GFR. It is currently unknown the predictive role of this abnormality toward cardiovascular events and death, independent of albuminuria and other known risk factors, in the diabetic population.

This observational study is aimed at assessing the association of reduced estimated GFR with cardiovascular morbidity and mortality in a large italian population (at least 15,000 subjects) of type 2 diabetic nondialytic outpatients over a 4-year follow-up.

Secondary endpoints are to assess in this population:

  • the prevalence and incidence of reduced GFR, as classified according to the National Kidney Foundation criteria, and its association with traditional cardiovascular risk factors;
  • the prevalence, incidence and cardiovascular predictivity of micro and macroalbuminuria.

Patients will be recruited from electronic records of 20 italian outpatients diabetic clinics.

Routine anamnestic, clinical, laboratory and instrumental data will be recorded at baseline and over 4 years to obtain information about:

  • renal function (albumin/creatinine ratio, serum creatinine with estimation of glomerular filtration rate [eGFR]);
  • cardiovascular risk factors (smoking, physical activity, family history of diabetes, dyslipidemia, hypertension and cardiovascular disease, BMI and waist circumference, total, LDL, HDL and non-HDL cholesterol, triglycerides, arterial blood pressure and HbA1c);
  • current glucose-, lipid- and blood pressure-lowering and anti-platelet or anti-coagulant treatment;
  • other illnesses;
  • cardiovascular events (myocardial infarction, stroke, lower limb ulcer/gangrene/amputation and coronary, carotid and lower limb revascularization, endovascular/surgical) and deaths.

These data will be derived from the electronic database of each participating center.

Laboratory analyses will be performed in each centre laboratory after proper standardization of analytical techniques.

Undersøgelsestype

Observationel

Tilmelding (Faktiske)

15628

Kontakter og lokationer

Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.

Studiesteder

      • Ascoli Piceno, Italien, 63100
        • Mazzoni Hospital, Division of Diabetology
      • Bari, Italien, 70124
        • Policlinico Hospital, Division of Endocrinology
      • Bergamo, Italien, 24128
        • Ospedali Riuniti di Bergamo, Division of Diabetology
      • Cagliari, Italien, 09042
        • Monserrato Hospital, Division of Diabetology
      • Catanzaro, Italien, 88100
        • Mater Domini Hospital, Division of Internal Medicine
      • Foggia, Italien, 71100
        • Policlinico Hospital, Division of Endocrinology
      • Latina, Italien, 04100
        • Santa Maria Goretti Hospital, Division of Diabetology
      • Milano, Italien, 20132
        • San Raffaele Hospital
      • Milano, Italien, 20122
        • Policlinico - Maggiore Hospital, Division of Endocrinology and Diabetology
      • Milano, Italien, 20123
        • San Giuseppe Hospital, Division of Endocrinology
      • Milano, Italien, 20142
        • San Paolo Hospital, Division of Internal Medicine
      • Orbassano-Torino, Italien, 10043
        • San Luigi Gonzaga Hospital, Division of Diabetes and Metabolic Diseases
      • Padova, Italien, 35128
        • Policlinico Hospital, Division of Diabetology
      • Pisa, Italien, 56124
        • Cisanello Hospital, Divisions of Diabetology
      • Pisa, Italien, 56126
        • Santa Chiara Hospital, Division of Internal Medicine
      • Rome, Italien, 00161
        • Policlinico Hospital, Division of Internal Medicine
      • Rome, Italien, 00189
        • Sant'Andrea Hospital, Division of Diabetology
      • Siena, Italien, 53100
        • Policlinico Le Scotte, Division of Diabetology
      • Torino, Italien, 10126
        • Le Molinette - San Giovanni Battista Hospital, Division of Diabetology
      • Verona, Italien, 37126
        • Maggiore Hospital, Division of Endocrinology and Metabolic Diseases

Deltagelseskriterier

Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.

Berettigelseskriterier

Aldre berettiget til at studere

40 år til 80 år (Voksen, Ældre voksen)

Tager imod sunde frivillige

Ingen

Køn, der er berettiget til at studere

Alle

Prøveudtagningsmetode

Sandsynlighedsprøve

Studiebefolkning

Outpatients clinics

Beskrivelse

Inclusion Criteria:

type 2 diabetes

Exclusion Criteria:

dyalisis or renal transplantation

Studieplan

Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Tidsramme
cardiovascular morbidity and mortality
Tidsramme: 4 years
4 years

Sekundære resultatmål

Resultatmål
Tidsramme
eGFR, as classified according to the National Kidney Foundation criteria
Tidsramme: 4 years
4 years
micro/macroalbuminuria
Tidsramme: 4 years
4 years
traditional cardiovascular risk factors
Tidsramme: 4 years
4 years

Samarbejdspartnere og efterforskere

Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.

Samarbejdspartnere

Efterforskere

  • Ledende efterforsker: Giuseppe Pugliese, MD, PhD, Diabetic Nephropathy Study Group
  • Studieleder: Anna Solini, MD, PhD, Diabetic Nephropathy Study Group

Publikationer og nyttige links

Den person, der er ansvarlig for at indtaste oplysninger om undersøgelsen, leverer frivilligt disse publikationer. Disse kan handle om alt relateret til undersøgelsen.

Generelle publikationer

Hjælpsomme links

Datoer for undersøgelser

Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.

Studer store datoer

Studiestart

1. juni 2008

Primær færdiggørelse (Faktiske)

1. november 2008

Studieafslutning (Faktiske)

1. februar 2015

Datoer for studieregistrering

Først indsendt

10. juli 2008

Først indsendt, der opfyldte QC-kriterier

10. juli 2008

Først opslået (Skøn)

15. juli 2008

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Skøn)

10. februar 2015

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

9. februar 2015

Sidst verificeret

1. februar 2015

Mere information

Begreber relateret til denne undersøgelse

Yderligere relevante MeSH-vilkår

Andre undersøgelses-id-numre

  • DNSG-SID 0601

Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .

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