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An Intervention to Examine the Effect of Vitamin D on Urine Protein Levels in Type 2 Diabetes

Intervention Using Vitamin D for Elevated Urinary ALbumin in Diabetes (IDEAL-2)

Status
UNKNOWN
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03216564
Acronym
IDEAL-2
Enrollment
320
Registered
2017-07-13
Start date
2017-05-10
Completion date
2019-05-10
Last updated
2018-09-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Diabetic Nephropathies

Brief summary

Diabetic kidney disease (nephropathy) develops in nearly 40% of patients with type 2 diabetes mellitus. Diabetic nephropathy is caused by damage to the small blood vessels in the kidneys due to uncontrolled blood sugar levels, which mean that the kidneys become less effective at filtering urine. This is associated with albuminuria (protein in the urine). Treatment with some drugs reduces the loss of albumin through the urine and delays disease progression. There is increasing evidence that vitamin D could also be important in management of diabetic kidney disease. The aim of this study is to investigate the efficacy and safety of a combined regimen of calcitriol (active vitamin D) and established drugs for diabetic kidney disease.

Detailed description

The investigators propose to test the efficacy and safety of a combined regimen of calcitriol and angiotensin converting enzyme inhibitor (ACEI) or angiotensin receptor blocker (ARB) in type 2 diabetes subjects with albuminuria. In the proposed study, the bioactive form of vitamin D (calcitriol) is being used for its ability to synergize with ACEI or ARB and prevent renal disease progression. The study expands on preliminary studies demonstrating a reduction in proteinuria with vitamin D analogue treatment, in subjects with both diabetic as well as non-diabetic kidney disease.

Interventions

DRUGCalcitriol

Active vitamin D (Calcitriol) 0.25 micrograms

Sponsors

Weill Cornell Medical College in Qatar
CollaboratorOTHER
Hamad Medical Corporation
Lead SponsorINDUSTRY

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

1. Age greater than or equal to 18 years and less than 80 years 2. Diagnosis of T2DM requiring treatment with at least one oral hypoglycaemic medication or insulin 2.1. Subjects will be considered to have established T2DM if the diagnosis of diabetes has been made and the subjects were treated with insulin or an oral hypoglycaemic agent for at least 6 months after diagnosis 2.2. Subjects will be considered to have newly established T2DM if the diagnosis of diabetes was diagnosed with a fasting plasma glucose ≥ 7 mmol/L (126 mg/dL) or haemoglobin A1c is \>6.5% in the past 6 months 3. Documented albuminuria defined as a presence of albuminuria on two occasions in the last six months: 3.1. Albumin ≥ 30 mg/24 hour in a 24 hour urine collection, or 3.2. Albumin ≥ 20 μg/min in a short-time urine collection, or 3.3. Albumin ≥ 30 mg/L in a spot urine sample, or 3.4. A spot-urine albumin-creatinine ration (ACR) ≥ 30 mg/g creatinine (≥ 2.5 mg/mmol creatinine in men, ≥ 3.5 mg/mmol creatinine in women) 4. Estimated glomerular filtration rate (eGFR) using the 4-variable Modification of Diet in Renal Disease (MDRD) equation of ≥ 25 mL/min/1.73 m2

Exclusion criteria

1. If female, positive pregnancy test or planning pregnancy in the subsequent 12 months 2. Pregnant 3. Breastfeeding 4. Corrected serum calcium ≥ 2.62 mmol/L 5. Serum Potassium \> 5.2 mmol/L if not on ACEI or ARB; Serum Potassium \> 6.0 mmol/L if on ACEI or ARB 6. 25-hydroxyvitamin D (25-OH Vit D) \> 80 ng/mL 7. PTH \> 200 pg/mL 8. Poorly controlled hypertension defined as systolic blood pressure ≥ 180 mm Hg or diastolic blood pressure ≥ 110 mm Hg 9. Systolic blood pressure (SBP) ≤ 110 mm Hg 10. History of kidney stones 11. History of severe chronic disease (e.g. chronic liver disease) 12. Active malignancy 13. Recent diagnosis of acute renal failure within 3 months of screening visit 14. Likelihood of renal replacement therapy within 1 year

Design outcomes

Primary

MeasureTime frameDescription
Urinary albumin creatinine ratio (ACR) measured biochemically26 weeksUrine albumin and creatinine will be measured biochemically and their ratio calculated

Secondary

MeasureTime frameDescription
24-hour urine albumin (24h UA) excretion26 weeks24-hour urine albumin (24h UA) excretion measured biochemically
Estimated glomerular filtration rate (eGFR)26 weeksCalculated using the Modification of Diet in Renal Disease (MDRD) equation
Blood pressure26 weeksBlood pressure measured using a digital sphygmomanometer

Other

MeasureTime frameDescription
Patient Reported Outcome: Quality of life26 weeksMeasured using the EQ5D questionnaire

Countries

Qatar

Contacts

Primary ContactShahrad Taheri, MB BS PhD
szt2004@qatar-med.cornell.edu0097444928998
Backup ContactMuhammad Asim, MB BS
Masim@hamad.qa0097455838342

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 7, 2026