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Clinical Trial Details

Trial ID: L2698
Source ID: NCT02105792
Associated Drug: Second- Or Third-Line Glucose-Lowering Diabetes Treatment
Title: PROMASTER - PROspective Cohort MRC ABPI STratification and Extreme Response Mechanism in Diabetes
Acronym: PROMASTER
Status: COMPLETED
Study Results: NO
Results:
Conditions: Diabetes
Interventions: DRUG: second- or third-line glucose-lowering diabetes treatment
Outcome Measures: Primary: Response to diabetes therapy, The primary outcome will be to compare the clinical characteristics of the patients who show an excellent response or a poor response to specific second- and third-line classes of treatment for Type 2 diabetes., Up to 9 months from commencement of new therapy | Secondary: Collection of samples for analysis of potential biomarkers, To collect a set of DNA, serum and urine samples to allow analysis of potential genetic and non genetic biomarkers for drug response and diabetes progression., within 9 months of recruitment date
Sponsor/Collaborators: Sponsor: Royal Devon and Exeter NHS Foundation Trust | Collaborators: University of Exeter|King's College London|King's College Hospital NHS Trust|University of Glasgow|NHS Greater Glasgow and Clyde|Newcastle University|Newcastle-upon-Tyne Hospitals NHS Trust|Oxford University Hospitals NHS Trust
Gender: ALL
Age: ADULT, OLDER_ADULT
Phases:
Enrollment: 820
Study Type: OBSERVATIONAL
Study Designs: Observational Model: |Time Perspective: p
Start Date: 2013-03
Completion Date: 2016-05
Results First Posted:
Last Update Posted: 2018-06-21
Locations: University of Exeter, Exeter, Devon, EX2 5DW, United Kingdom|Oxford University Hospitals NHS Trust, Oxford, Oxfordshire, OX3 7LE, United Kingdom|University of Newcastle, Newcastle upon Tyne, Tyne And Wear, NE1 7RU, United Kingdom|University of Glasgow, Glasgow, G12 8TA, United Kingdom|King's College University of London, London, SE1 9NH, United Kingdom
URL: https://clinicaltrials.gov/show/NCT02105792