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
Clinicaltrials.gov ID
Not applicable
EudraCT ID
Not applicable
EU CT Number
Not applicable
Trial status
Study complete
Study complete
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:
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.
- reference RECORD NCT00379769
- reference RECORD NCT00379769
Inclusion and exclusion criteria
Inclusion criteria:
- reference RECORD NCT00379769
Exclusion criteria:
- 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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