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Adolescent type 1 diabetes cardio-renal intervention trial
Source of recordUK Trials
ISRCTNISRCTN91419926
Date ISRCTN assigned03/10/2007
Local reference number(s)RP06
Public titleAdolescent type 1 diabetes cardio-renal intervention trial
Scientific title
AcronymAdolescent Diabetes Intervention Trial (AdDIT)
Disease/condition/study domainType 1 diabetes
Study hypothesisTo determine whether intervention with Angiotensin Converting Enzyme Inhibitors (ACEI), statins, or a combination of both, when compared with placebo, will:
1. Reduce albumin excretion as assessed by six monthly measurement of Albumin/Creatinine Ratio (ACR) in three early morning urines
2. Reduce the incidence of Microalbuminuria (MA) (ACR log mean greater than 3.5 mg/mmol (males) or greater than 4 mg/mmol [females] in two out of three urines) at the end of the study period
3. Reduce the incidence of MA during the six month run out period following the completion of intervention phase
Design/methodologyRandomised, controlled, double blind, clinical trial
Research ethics reviewEthics approval submitted in August 2007.
Countries of trialUnited Kingdom, Australia, Canada
Participants - inclusion criteria1. Type 1 diabetes diagnosed for greater than one year
2. Aged 11 to 15 years
3. High risk for the development of diabetic nephropathy and Cardiovascular Disease (CVD) as predicted by albumin excretion in the upper tertile after appropriate adjustment for age, sex, age at diagnosis and duration of disease
Participants - exclusion criteria1. Non-type 1 diabetes, i.e., type 2 diabetes, insulin dependent diabetes related to monogenic disease, secondary diabetes
2. ACR based on six early morning urines deemed to be at low risk for subsequent development of CVD or diabetic nephropathy
3. Pregnancy, or unwillingness to comply with contraceptive advice and regular pregnancy testing throughout the trial
4. Severe hyperlipidaemia and family history data to support diagnosis of familial hypercholesterolaemia
5. Established hypertension unrelated to diabetic nephropathy
6. Prior exposure to the investigational products, statins and ACEI
Patient information material
Anticipated start date01/01/2008
Anticipated end date31/12/2012
Status of trialOngoing
Target number of participants500
InterventionsFour arm randomisation:
1. Quinapril, 5 - 10 mg daily and placebo
2. Atorvostatin, 10 mg daily and placebo
3. Quinapril and atorvostatin
4. Placebo

The duration of study will be three to four years, that is until subjects reach the age of 14 to 18 years and they will also be studied for an additional six months during the run out period.
Primary outcome measure(s)The primary endpoint is defined as the area under the curve over time of log albumin-creatinine ratio per year, with standardisation for gender, age and duration of disease.
Secondary outcome measure(s)1. Changes in carotid intimal media thickness, between baseline and the end of intervention period
2. Changes in arterial Blood Pressure (BP), lipids and other lipoproteins, CVD risk markers (high-sensitive C-Reactive Protein [hsCRP] and Asymmetric Dimethylarginine [ADMA]), assessed every six months during the intervention period
3. Changes in measures of Glomerular Filtration Rate (GFR) (plasma Symmetrical Dimethylarginine [SDMA], creatinine and cystatin C) assessed every six months during the intervention period
4. Changes in quality of life and health economics
Sources of funding1. Diabetes UK (UK) (ref: RD06/0003341)
2. Juvenile Diabetes Research Foundation (UK) (ref: 8-2007-902)
3. British Heart Foundation (UK) (ref: SP/07/002/23394)
Sponsor nameUniversity of Cambridge and Cambridge University Hospitals NHS Foundation Trust (UK)
Sponsor detailsResearch Service Division
16 Mill Lane
Cambridge
United Kingdom
CB2 1SB
Sponsor emailhelen.atkinson@rsd.cam.ac.uk
Sponsor websitehttp://www.cam.ac.uk/
Contact nameProf David Dunger
Contact detailsUniversity Department of Paediatrics
Box 116, Addenbrooke's Hospital
Cambridge
United Kingdom
CB2 0QQ
Contact emaildbd25@cam.ac.uk
More informationFor more up-to-date information please go to the ISRCTN link below.
Link to record in ISRCTN RegisterISRCTN91419926
Date last extracted from ISRCTN register17/04/2008
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