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Trial details imported from ClinicalTrials.gov

For full trial details, please see the original record at https://clinicaltrials.gov/ct2/show/NCT00252733




Registration number
NCT00252733
Ethics application status
Date submitted
10/11/2005
Date registered
15/11/2005
Date last updated
14/05/2014

Titles & IDs
Public title
Diabetic Retinopathy Candesartan Trials
Scientific title
Effects of Candesartan Cilexetil (Candesartan) on Diabetic Retinopathy in Type 1 Diabetic Patients Without Retinopathy.
Secondary ID [1] 0 0
DIRECT
Secondary ID [2] 0 0
D2453C00045
Universal Trial Number (UTN)
Trial acronym
DIRECT
Linked study record

Health condition
Health condition(s) or problem(s) studied:
Type 1 Diabetes 0 0
Condition category
Condition code
Metabolic and Endocrine 0 0 0 0
Diabetes
Eye 0 0 0 0
Diseases / disorders of the eye

Intervention/exposure
Study type
Interventional
Description of intervention(s) / exposure
Treatment: Drugs - candesartan cilexetil

No Intervention: 1 - Placebo

Experimental: 2 - candesartan cilexetil


Treatment: Drugs: candesartan cilexetil
32 mg once daily oral tablet given over 60 months
Intervention code [1] 0 0
Treatment: Drugs
Comparator / control treatment
Control group

Outcomes
Primary outcome [1] 0 0
Number of Participants With a 2-step or Greater Increase in Early Treatment Diabetic Retinopathy Study (ETDRS) Severity Scale.
Timepoint [1] 0 0
From baseline to end of study, i.e. 5 years, with visits after a half year, one year and thereafter one visit per year.
Secondary outcome [1] 0 0
Rate of Change in Urinary Albumin Excretion Rate (UAER).
Timepoint [1] 0 0
From baseline to end of study, i.e. 5 years.

Eligibility
Key inclusion criteria
- Type 1 diabetes diagnosed before age of 36 years and in need for continuous insulin
treatment within 1 year of diagnosis of diabetes are included.

- Duration of diabetes for > 1 year and < 15 years with stable diabetic therapy within
last 6 months.

- Patients with untreated resting mean sitting SBP < 130 mmHg, mean sitting DBP < 85
mmHg and with retinal photograph grading level 10/10 (on ETDRS severity scale).
Minimum age
18 Years
Maximum age
50 Years
Sex
Both males and females
Can healthy volunteers participate?
No
Key exclusion criteria
- Patients with the following conditions are excluded from participation in the study:

- Cataract or media opacity of a degree which precludes taking gradable retinal
photographs

- Angle closure glaucoma, which precludes pharmacological dilatation of the pupil

- History of retinopathy

- History or presence of clinical significant macular oedema (CSME)

- History or evidence of photocoagulation of the retina Other retinal conditions which
may mask assessment, eg, retinal vein occlusion

- Positive micral dipstick test

- Presence of secondary diabetes

- Pregnant or lactating women or women of child bearing potential not practicing an
adequate method of contraception

- Need of treatment with ACE-inhibitor

- Haemodynamically significant aortic or mitral valve stenosis

- Known renal artery stenosis or kidney transplantation

- Hypersensitivity to study drug

- Severe concomitant disease which may interfere with the assessment of the patient, eg,
malignancy, as judged by the investigator

Study design
Purpose of the study
Treatment
Allocation to intervention
Randomised controlled trial
Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Masking / blinding
Blinded (masking used)
Who is / are masked / blinded?
The people receiving the treatment/s
The people administering the treatment/s
The people assessing the outcomes
The people analysing the results/data
Intervention assignment
Parallel
Other design features
Phase
Phase 3
Type of endpoint/s
Statistical methods / analysis

Recruitment
Recruitment status
Completed
Data analysis
Reason for early stopping/withdrawal
Other reasons
Date of first participant enrolment
Anticipated
Actual
1/06/2001
Date of last participant enrolment
Anticipated
Actual
Date of last data collection
Anticipated
Actual
1/04/2008
Sample size
Target
Accrual to date
Final
5238
Recruitment in Australia
Recruitment state(s)
Recruitment hospital [1] 0 0
Research Site - Herston
Recruitment hospital [2] 0 0
Research Site - Perth
Recruitment postcode(s) [1] 0 0
- Herston
Recruitment postcode(s) [2] 0 0
- Perth
Recruitment outside Australia
Country [1] 0 0
Denmark
State/province [1] 0 0
Odense

Funding & Sponsors
Primary sponsor type
Commercial sector/Industry
Name
AstraZeneca
Address
Country
Other collaborator category [1] 0 0
Commercial sector/Industry
Name [1] 0 0
Takeda
Address [1] 0 0
Country [1] 0 0

Ethics approval
Ethics application status

Summary
Brief summary
The primary objective is to determine whether candesartan, compared to placebo reduces the
incidence of diabetic retinopathy in normotensive, normoalbuminuric type 1 diabetic patients
without retinopathy.

The secondary objective is to determine whether candesartan, compared to placebo,
beneficially influences the rate of change in urinary albumin excretion rate (UAER).

This study is part of the DIRECT Programme also including secondary prevention studies of
diabetic retinopathy in both type 1 and type 2 diabetes. The primary objective for all three
pooled studies is to determine whether candesartan, compared to placebo, reduces the
incidence of microalbuminuria in type 1 and type 2 diabetic patients.
Trial website
https://clinicaltrials.gov/ct2/show/NCT00252733
Trial related presentations / publications
Public notes

Contacts
Principal investigator
Name 0 0
AstraZeneca Atacand Medical Science Director, MD
Address 0 0
AstraZeneca
Country 0 0
Phone 0 0
Fax 0 0
Email 0 0
Contact person for public queries
Name 0 0
Address 0 0
Country 0 0
Phone 0 0
Fax 0 0
Email 0 0
Contact person for scientific queries



Summary Results

For IPD and results data, please see https://clinicaltrials.gov/ct2/show/NCT00252733