Last updated: 11/07/2018 08:55:19

Blinded, Re-adjudication of Mortality and Major Cardiovascular Endpoints (MACE) from the Rosiglitazone Evaluated for Cardiovascular Outcomes and Regulation of glycaemia in Diabetes trial (RECORD)RECORD

GSK study ID
115170
Clinicaltrials.gov ID
Not applicable
EudraCT ID
Not applicable
EU CT Number
Not applicable
Trial status
Study complete
Study complete
Overview
Eligibility
Locations
Study documents
Results summary
Plain language summaries
Additional information

Trial overview

Official title: Blinded, Re-adjudication of Mortality and Major Cardiovascular Endpoints (MACE) from the Rosiglitazone Evaluated for Cardiovascular Outcomes and Regulation of glycaemia in Diabetes trial (RECORD)
Trial description: This study will independently re-adjudicate and re-analyze mortality and major adverse cardiovascular events (MACE) reported during the RECORD trial. The RECORD trial was an open-label, randomized trial comparing rosiglitazone-containing combination therapy for type 2 diabetes with the most commonly used dual oral combination of metformin and a sulfonylurea. The results of the RECORD study [NCT00379769] together with other data were reviewed and discussed at a July 13-14, 2010 joint meeting of the Food and Drug Administration’s (FDA) Endocrinology and Metabolic Drugs Advisory Committee and the Drug Safety and Risk Management Advisory Committee. Following the review, the FDA required GSK to commission an independent, patient record level, re-adjudication of all cause deaths and deaths due to cardiovascular reasons, as well as non-fatal myocardial infarction and non fatal stroke. This will be conducted in a stepwise manner with initial examination of the mortality finding; if the mortality finding is determined to be valid by the FDA, then the other MACE elements will be adjudicated.
Primary purpose:
Other
Trial design:
Parallel Assignment
Masking:
Double (Investigator, Outcomes Assessor)
Allocation:
Randomized
Primary outcomes:

CV mortality

Timeframe: Baseline through End of Study (up to 7.5 years)

All cause mortality

Timeframe: Baseline through End of Study (up to 7.5 years)

Secondary outcomes:

MACE

Timeframe: Baseline through End of Study (up to 7.5 years)

Myocardial infarction

Timeframe: Baseline through End of Study (up to 7.5 years)

Stroke

Timeframe: Baseline through End of Study (up to 7.5 years)

Interventions:
  • Drug: Metformin
  • Drug: Sulfonylurea
  • Drug: Rosiglitazone
  • Enrollment:
    1
    Primary completion date:
    Not applicable
    Observational study model:
    Not applicable
    Time perspective:
    Not applicable
    Clinical publications:
    Lopes RD, Dickerson S, Hafley G, Burns S, Tourt-Uhlig S, White J, Newby LK, Komajda M, McMurray J, Bigelow R, Home PD, Mahaffey KW.Methodology of a re-evaluation of cardiovascular outcomes in the RECORD trial: Study design and conduct.Am Heart J.2013;166(2):208-216.e28.
    Medical condition
    Diabetes Mellitus, Type 2
    Product
    rosiglitazone
    Collaborators
    Duke Clinical Research Institute
    Study date(s)
    January 2011 to February 2012
    Type
    Observational
    Phase
    4

    Participation criteria

    Sex
    Female & Male
    Age
    40 - 75 Year
    Accepts healthy volunteers
    none
    • reference RECORD NCT00379769
    • reference RECORD NCT00379769

    Trial location(s)

    This study does not involve prospective enrollment of participants.

    Study documents

    Clinical study report
    Available language(s): English
    Scientific result summary
    Available language(s): English

    If you wish to request for full study report, please contact - [email protected]

    Results overview

    Refer to study documents

    Recruitment status
    Study complete
    Actual primary completion date
    Not applicable
    Actual study completion date
    2012-17-02

    Plain language summaries

    Not applicable. GSK’s transparency policy provides for Plain Language Summaries for Interventional studies.

    Additional information about the trial

    Not applicable
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