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Colchicine for Diabetic Nephropathy Trial (CDNT)

Primary Purpose

Diabetic Nephropathies

Status
Unknown status
Phase
Phase 1
Locations
Israel
Study Type
Interventional
Intervention
Colchicine
Placebo
Sponsored by
Sheba Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Diabetic Nephropathies

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Patients with diabetes mellitus , age>18 years old, able to sign an informed consent.
  2. Hemoglobin A1c in the range of 6-9%, stable for last year (0.5±)
  3. Blood creatinine lower than 2 mg/dL.
  4. Blood pressure lower than 140/90 mmHg on stable anti-hypertensive treatment for at least 3 months.
  5. Treated with ACE or angiotensin II receptor blocker , unless contraindicated

Exclusion Criteria:

  1. Malignancy or significant heart, lung or liver disease.
  2. Any GI disease, inflammatory bowel disease , malnutrition ( BMI under 18 )
  3. Psychiatric disease
  4. Any muscle disease, history of rhabdomyolysis , myopathy or myositis.
  5. Any disease causing renal injury/proteinuria apart from diabetes mellitus
  6. Any inflammatory or autoimmune disease
  7. Any infection during the last month.

Sites / Locations

  • Sheba Medical CenterRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Colchicine

Placebo

Arm Description

20 patients will receive up to 2 mg of colchicine for 18 months

20 patients will receive placebo for 18 months

Outcomes

Primary Outcome Measures

Change of urinary protein excretion ( mg/24hrs) from baseline to 18 months.

Secondary Outcome Measures

Full Information

First Posted
April 30, 2015
Last Updated
May 6, 2017
Sponsor
Sheba Medical Center
Collaborators
D-Cure, Israel
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1. Study Identification

Unique Protocol Identification Number
NCT02442921
Brief Title
Colchicine for Diabetic Nephropathy Trial
Acronym
CDNT
Official Title
The Effect of Colchicine Treatment on the Progression of Proteinuria in Patients With Diabetic Nephropathy.
Study Type
Interventional

2. Study Status

Record Verification Date
May 2017
Overall Recruitment Status
Unknown status
Study Start Date
February 22, 2016 (Actual)
Primary Completion Date
April 30, 2019 (Anticipated)
Study Completion Date
April 30, 2019 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Sheba Medical Center
Collaborators
D-Cure, Israel

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Forty patients with diabetic nephropathy will be treated with colchicine up to 2 mg, or placebo, for 18 months. A follow up will be performed after 12 additional months. The primary outcome will be a significant reduction or stabilization of proteinuria during the 18 month treatment period.
Detailed Description
Diabetic nephropathy is the leading cause today for end stage renal failure in the western world. Multifactorial intervention in patients may slow the rate of albuminuria and renal injury; however several new drug trials have failed so far to significantly attenuate its progression. Several pathways are identified in the development of diabetic nephropathy, however, in recent years many researchers suspect that inflammatory pathways play central roles in the progression of diabetic neuropathy . There is compelling evidence that diabetes mellitus has an auto-inflammatory component with Nlrp3 inflammasome and interleukin -1 β activation. Colchicine is a relatively safe anti-inflammatory drug used to treat and reverse albuminuria in familial Mediterranean fever nephropathy, an auto-inflammatory disease. Data from one study demonstrated that colchicine diminished proteinuria and inflammation in experimental-diabetic animal models. Working hypothesis and aims: To assess whether colchicine reduces proteinuria in diabetic patients with diabetic neuropathy , despite maximal multi-factorial interventions (angiotensin-converting-enzyme inhibitors, tight glycemic and hypertensive control, lifestyle intervention, etc.). Methods: Forty patients with stable diabetes, and diabetic neuropathy with proteinuria of 0.5-6g/24 hours, despite standard treatment, will receive colchicine (n=20) or placebo (n=20) for 18 months. Urinary protein and creatinine clearance will be assessed three months before the study initiation, at baseline and every three months thereafter. Blood creatinine, complete blood count, creatine phosphokinase , liver function tests, fasting Glucose Test, HbA1c, and urine protein/creatinine ratio and diabetes mellitus treatment monitoring and follow-up will be performed every three months. Oral colchicine treatment will be initiated at 1mg per day, and increased gradually to 2 mg, if gastrointestinal or musculoskeletal disturbances are absent or tolerated. The participants will be called and evaluated a year after the end of treatment for all parameters mentioned. Statistical analysis will be performed by a statistician. Expected results: A significant reduction or stabilization of proteinuria during the 18 month treatment period, or at follow up at one year later. Importance and Relevance to the call This study may define a new treatment for diabetic nephropathy.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diabetic Nephropathies

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1, Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
40 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Colchicine
Arm Type
Experimental
Arm Description
20 patients will receive up to 2 mg of colchicine for 18 months
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
20 patients will receive placebo for 18 months
Intervention Type
Drug
Intervention Name(s)
Colchicine
Intervention Description
up to 2mg of Colchicine daily
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
Daily placebo
Primary Outcome Measure Information:
Title
Change of urinary protein excretion ( mg/24hrs) from baseline to 18 months.
Time Frame
From baseline to 18 months ( end of trial )

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients with diabetes mellitus , age>18 years old, able to sign an informed consent. Hemoglobin A1c in the range of 6-9%, stable for last year (0.5±) Blood creatinine lower than 2 mg/dL. Blood pressure lower than 140/90 mmHg on stable anti-hypertensive treatment for at least 3 months. Treated with ACE or angiotensin II receptor blocker , unless contraindicated Exclusion Criteria: Malignancy or significant heart, lung or liver disease. Any GI disease, inflammatory bowel disease , malnutrition ( BMI under 18 ) Psychiatric disease Any muscle disease, history of rhabdomyolysis , myopathy or myositis. Any disease causing renal injury/proteinuria apart from diabetes mellitus Any inflammatory or autoimmune disease Any infection during the last month.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Shaye Kivity, MD
Phone
0526668143
Email
kivitys@gmail.com
First Name & Middle Initial & Last Name or Official Title & Degree
Naomi Friedman, Ms.c
Email
naomi.friedman@sheba.health.gov.il
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Shaye Kivity, MD
Organizational Affiliation
Sheba Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Sheba Medical Center
City
Ramat Gan
ZIP/Postal Code
52621
Country
Israel
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Shaye Kivity, MD
Phone
0526668134
Email
kivitys@gmail.com
First Name & Middle Initial & Last Name & Degree
Naomi Friedman, M.sc
Phone
+972544451556
Email
naomi.friedman@sheba.health.gov.il

12. IPD Sharing Statement

Plan to Share IPD
Yes

Learn more about this trial

Colchicine for Diabetic Nephropathy Trial

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