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Does Saxagliptin Reduce the Risk of Cardiovascular Events When Used Alone or Added to Other Diabetes Medications (SAVOR- TIMI 53)

9. juli 2014 opdateret af: AstraZeneca

A Multicentre, Randomised, Double-Blind, Placebo-Controlled Phase IV Trial to Evaluate the Effect of Saxagliptin on the Incidence of Cardiovascular Death, Myocardial Infarction or Ischaemic Stroke in Patients With Type 2 Diabetes

The purpose of this study is to determine whether saxagliptin can reduce the risk of cardiovascular events when used alone or added to other diabetes medications

Studieoversigt

Status

Afsluttet

Detaljeret beskrivelse

A Multicentre, Randomised, Double-Blind, Placebo-Controlled Phase IV Trial to Evaluate the Effect of Saxagliptin on the Incidence of Cardiovascular Death, Myocardial Infarction or Ischaemic Stroke in Patients with Type 2 Diabetes

Undersøgelsestype

Interventionel

Tilmelding (Faktiske)

18206

Fase

  • Fase 4

Kontakter og lokationer

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

Studiesteder

      • Buenos Aires, Argentina
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      • Ciudad Autonom de Buenos Aires, Argentina
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        • Research Site
      • Tijuana, Mexico
        • Research Site
      • Xalapa, Mexico
        • Research Site
      • Callao, Peru
        • Research Site
      • Lima, Peru
        • Research Site
      • San Isidro, Peru
        • Research Site
      • Bydgoszcz, Polen
        • Research Site
      • Gdansk, Polen
        • Research Site
      • Kamieniec Ząbkowicki, Polen
        • Research Site
      • Koluszki, Polen
        • Research Site
      • Krakow, Polen
        • Research Site
      • Lodz, Polen
        • Research Site
      • Mrgowo, Polen
        • Research Site
      • Nakso nad Noteci, Polen
        • Research Site
      • Opole, Polen
        • Research Site
      • Oława, Polen
        • Research Site
      • Poznan, Polen
        • Research Site
      • Przemyśl, Polen
        • Research Site
      • Sieradz, Polen
        • Research Site
      • Skierniewice, Polen
        • Research Site
      • Toruń, Polen
        • Research Site
      • Warszawa, Polen
        • Research Site
      • Wroclaw, Polen
        • Research Site
      • Wrocław, Polen
        • Research Site
      • Wąbrzeźno, Polen
        • Research Site
      • Zabrze, Polen
        • Research Site
      • Łęczna, Polen
        • Research Site
      • Aguas Buneas, Puerto Rico
        • Research Site
      • Bayamon, Puerto Rico
        • Research Site
      • Cidra, Puerto Rico
        • Research Site
      • Hato Rey, Puerto Rico
        • Research Site
      • Jardines de Loiza, Loiza, Puerto Rico
        • Research Site
      • Juncos, Puerto Rico
        • Research Site
      • Ponce, Puerto Rico
        • Research Site
      • Rio Piedras, Puerto Rico
        • Research Site
      • San Juan, Puerto Rico
        • Research Site
      • Toa Baja, Puerto Rico
        • Research Site
      • Alicante, Spanien
        • Research Site
      • Barcelona, Spanien
        • Research Site
      • Granada, Spanien
        • Research Site
      • Jerez de la Frontera Cadiz, Spanien
        • Research Site
      • Lérida, Spanien
        • Research Site
      • Madrid, Spanien
        • Research Site
      • Majadahonda, Spanien
        • Research Site
      • Oviedo, Spanien
        • Research Site
      • Palma de Mallorca, Spanien
        • Research Site
      • Santiago de Compostela, Spanien
        • Research Site
      • Sevilla, Spanien
        • Research Site
      • Valencia, Spanien
        • Research Site
      • Brämhult, Sverige
        • Research Site
      • Eksjö, Sverige
        • Research Site
      • Goteborg, Sverige
        • Research Site
      • Göteborg, Sverige
        • Research Site
      • Helsingborg, Sverige
        • Research Site
      • Jönköping, Sverige
        • Research Site
      • Malmo, Sverige
        • Research Site
      • Rättvik, Sverige
        • Research Site
      • Stockholm, Sverige
        • Research Site
      • Söråker, Sverige
        • Research Site
      • Umeå, Sverige
        • Research Site
      • Örebro, Sverige
        • Research Site
      • Östersund, Sverige
        • Research Site
      • Benoni, Sydafrika
        • Research Site
      • Cape Town, Sydafrika
        • Research Site
      • Durban, Sydafrika
        • Research Site
      • Johannesburg, Sydafrika
        • Research Site
      • Parow, Sydafrika
        • Research Site
      • Pretoria, Sydafrika
        • Research Site
      • Umkomaas, Sydafrika
        • Research Site
      • Verulam, Sydafrika
        • Research Site
      • Kaohsiung, Taiwan
        • Research Site
      • Kaohsiung Hsien, Taiwan
        • Research Site
      • Taichung, Taiwan
        • Research Site
      • Taipei, Taiwan
        • Research Site
      • Yong-Kang City, Taiwan
        • Research Site
      • Bangkok, Thailand
        • Research Site
      • Bangkoknoi, Thailand
        • Research Site
      • Chiang Mai, Thailand
        • Research Site
      • Khon Kaen, Thailand
        • Research Site
      • Ratchaburi, Thailand
        • Research Site
      • Beroun, Tjekkiet
        • Research Site
      • Blansko, Tjekkiet
        • Research Site
      • Breclav, Tjekkiet
        • Research Site
      • Brno, Tjekkiet
        • Research Site
      • Caslav, Tjekkiet
        • Research Site
      • Cheb, Tjekkiet
        • Research Site
      • Chrudim III, Tjekkiet
        • Research Site
      • Havirov, Tjekkiet
        • Research Site
      • Hodonin, Tjekkiet
        • Research Site
      • Horovice, Tjekkiet
        • Research Site
      • Hradec Kralove, Tjekkiet
        • Research Site
      • Jablonec nad Nisou, Tjekkiet
        • Research Site
      • Kromeriz, Tjekkiet
        • Research Site
      • Olomouc-Lazce, Tjekkiet
        • Research Site
      • Ostrava, Tjekkiet
        • Research Site
      • Ostrava - Belsky les, Tjekkiet
        • Research Site
      • Ostrava - Kuncice, Tjekkiet
        • Research Site
      • Ostrava-Vitkovice, Tjekkiet
        • Research Site
      • Pardubice, Tjekkiet
        • Research Site
      • Plzen, Tjekkiet
        • Research Site
      • Praha, Tjekkiet
        • Research Site
      • Praha 2, Tjekkiet
        • Research Site
      • Praha 6, Tjekkiet
        • Research Site
      • Prelouc, Tjekkiet
        • Research Site
      • Slany, Tjekkiet
        • Research Site
      • Uherske Hradiste, Tjekkiet
        • Research Site
      • Valaske Klobouky, Tjekkiet
        • Research Site
      • Zlin, Tjekkiet
        • Research Site
      • Aschaffenburg, Tyskland
        • Research Site
      • Bad Nauheim, Tyskland
        • Research Site
      • Bad Oeynhausen, Tyskland
        • Research Site
      • Berlin, Tyskland
        • Research Site
      • Deggingen, Tyskland
        • Research Site
      • Dippoldiswalde, Tyskland
        • Research Site
      • Dortmund, Tyskland
        • Research Site
      • Dresden, Tyskland
        • Research Site
      • Eschweiler, Tyskland
        • Research Site
      • Gießen, Tyskland
        • Research Site
      • Goch, Tyskland
        • Research Site
      • Gueglingen, Tyskland
        • Research Site
      • Hamburg, Tyskland
        • Research Site
      • Hohenmölsen, Tyskland
        • Research Site
      • Kassel, Tyskland
        • Research Site
      • Leipzig, Tyskland
        • Research Site
      • Mayen, Tyskland
        • Research Site
      • Rehlingen Siersburg, Tyskland
        • Research Site
      • Rotenburg, Tyskland
        • Research Site
      • Balatonfüred, Ungarn
        • Research Site
      • Budapest, Ungarn
        • Research Site
      • Békéscsaba, Ungarn
        • Research Site
      • Cegled, Ungarn
        • Research Site
      • Csongrad, Ungarn
        • Research Site
      • Eger, Ungarn
        • Research Site
      • Gyor, Ungarn
        • Research Site
      • Gyula, Ungarn
        • Research Site
      • Gyöngyös, Ungarn
        • Research Site
      • Miskolc, Ungarn
        • Research Site
      • Nagykanizsa, Ungarn
        • Research Site
      • Pecs, Ungarn
        • Research Site
      • Siofok, Ungarn
        • Research Site
      • Szolnok, Ungarn
        • Research Site
      • Veszprém, Ungarn
        • Research Site

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 og ældre (Voksen, Ældre voksen)

Tager imod sunde frivillige

Ingen

Køn, der er berettiget til at studere

Alle

Beskrivelse

Inclusion Criteria:

  • Patients with type 2 diabetes mellitus
  • HbA1c ≥6.5%. (based on the last measured and documented laboratory measurement within 6 months)
  • High risk for CV events -Established cardiovascular disease and/or multiple risk factors

Exclusion Criteria:

  • Current or previous (within 6 months) treatment with DPP4 inhibitors and/or GLP-1 mimetics
  • Acute vascular event <2months prior to randomisation

Studieplan

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

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

  • Primært formål: Behandling
  • Tildeling: Randomiseret
  • Interventionel model: Parallel tildeling
  • Maskning: Firedobbelt

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Placebo komparator: Placebo
Eksperimentel: Saxagliptin
5 mg or 2.5 mg once daily
Andre navne:
  • Onglyza

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Participants With Any Event From the Composite of Cardiovascular Death (CV Death), Non-fatal Myocardial Infarction (MI), or Non-fatal Ischaemic Stroke
Tidsramme: Randomization (day 0) up to 2.9 years
Participants with CV death, non-fatal MI or non-fatal ischaemic stroke. If no event, censoring occurs at the patient withdrawal of consent, last contact, or death (when applicable)-whichever was later.
Randomization (day 0) up to 2.9 years

Sekundære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Participants With Any Event From the Composite of CV Death, Non-fatal MI, Non-fatal Ischaemic Stroke, Hospitalisation for Heart Failure, Hospitalisation for Unstable Angina Pectoris, or Hospitalisation for Coronary Revascularisation
Tidsramme: Randomization (day 0) up to 2.9 years
Participants with CV death, non-fatal MI, non-fatal ischaemic stroke, hospitalisation for heart failure, hospitalisation for unstable angina pectoris, or hospitalisation for coronary revascularisation. If no event, censoring occurs at the patient withdrawal of consent, last contact, or death (when applicable)-whichever was later.
Randomization (day 0) up to 2.9 years
Participants With Event of Death
Tidsramme: Randomization (day 0) up to 2.9 years
Participants with event of death. If no event, censoring occurs at the patient withdrawal of consent, or last contact -whichever was later.
Randomization (day 0) up to 2.9 years

Samarbejdspartnere og efterforskere

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

Sponsor

Samarbejdspartnere

Efterforskere

  • Studiestol: Eugene Braunwald, TIMI
  • Ledende efterforsker: Itamar Raz, Hadassah Medical Organization
  • Ledende efterforsker: Deepak Bhatt, TIMI

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

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. maj 2010

Primær færdiggørelse (Faktiske)

1. maj 2013

Studieafslutning (Faktiske)

1. maj 2013

Datoer for studieregistrering

Først indsendt

25. marts 2010

Først indsendt, der opfyldte QC-kriterier

20. april 2010

Først opslået (Skøn)

21. april 2010

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Skøn)

17. juli 2014

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

9. juli 2014

Sidst verificeret

1. juli 2014

Mere information

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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