search
Back to results

Queen's University Investigation of Calcification in Chronic Kidney Disease (QUICK)

Primary Purpose

Chronic Kidney Disease

Status
Completed
Phase
Phase 3
Locations
Canada
Study Type
Interventional
Intervention
Bisphosphonate
Placebo
Sponsored by
Queen's University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Chronic Kidney Disease focused on measuring Chronic Kidney Failure, Vascular Calcification, Bisphosphonates

Eligibility Criteria

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

Inclusion Criteria:

  • 18 years of age
  • receiving maintenance renal replacement therapy for less than 12 months
  • incident patients starting renal replacement therapy for the first time

Exclusion Criteria:

  • active vasculitis
  • severe hypocalcemia
  • previous adverse side effect to bisphosphonate use
  • current use of corticosteroids
  • weight greater than 300 pounds
  • pregnancy
  • not expected to survive greater than one year
  • expected to discontinue renal replacement therapy during the study period or recover renal function
  • evidence of adynamic bone disease
  • current bisphosphonate use

Sites / Locations

  • Kingston General Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

1

2

Arm Description

Arm #1 will include patients randomized to receive bisphosphonate therapy for 24 months.

Arm #2 will include patients randomized to receive placebo therapy for 24 months

Outcomes

Primary Outcome Measures

Absolute change in coronary artery calcification score (CaSc) from baseline to study completion.

Secondary Outcome Measures

Change in bone density score (wrist/hip) as calculated by Ct scanning method, # fractures, MI, Stroke, amputation/surgery for peripheral revascularization.

Full Information

First Posted
May 28, 2008
Last Updated
September 25, 2015
Sponsor
Queen's University
search

1. Study Identification

Unique Protocol Identification Number
NCT00687661
Brief Title
Queen's University Investigation of Calcification in Chronic Kidney Disease
Acronym
QUICK
Official Title
The Use of Bisphosphonates to Prevent or Delay the Progression of Vascular Calcification in End-Stage Renal Disease: A Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
September 2015
Overall Recruitment Status
Completed
Study Start Date
October 2008 (undefined)
Primary Completion Date
June 2013 (Actual)
Study Completion Date
June 2013 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Queen's University

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Kidney disease is a fundamental part of medicine because of its prominence in Western society. Common conditions such as diabetes, hypertension and kidney infections can all progress to End-Stage Renal Disease (ESRD) also known as Stage 5 chronic kidney disease (CKD 5). Once ESRD has begun, kidney function is poor at best, thus the body is unable to effectively clear harmful toxins from the blood. A common feature of ESRD is vascular calcification, a process where blood vessels (especially arteries) attract deposits of the mineral calcium. Over time, these deposits harden and thicken in the layers of blood vessels, which limit blood flow to body tissues and can produce significant disease including hypertension, heart disease and stroke. Although the process of vascular calcification is unknown, there is mounting evidence that it is mediated by cellular events that are similar to those seen in bone formation with in the body (osteogenesis). With this point in mind, it has been suggested that agents medicine employs to limit excess bone formation will reduce the rate of vascular calcification in CKD Stage 5. This study will employ one group of drugs called bisphosphonates which have been used to limit bone formation. It will study their effect on vascular calcification in adult dialysis patients.
Detailed Description
Presently, there exist few therapies aimed at retarding the progression of vascular calcification. One study showed that agents that limit the absorption of phosphate from food (phosphate binders) slow the progression of vascular calcification, and as a result, treatments emphasize phosphate control through diet and phosphate binders. Other studies have shown that the use of statins, to lower LDL cholesterol levels may reduce the progression of coronary calcification in non-ESRD patients, but data from ESRD are lacking. While these treatments have been helpful, the improvements in patients' outcomes have not been overwhelming positive. This proposed study is not the first to study the use of bisphosphonates on vascular calcification. Repeated studies have shown impressive reduction in calcification rates in several animal models, which begs the question, how will bisphosphonates fare in human subjects? Preliminary research has begun, but clearly an expansive trial on humans is needed to explore the use of a promising therapy. Our study hopes to provide insight into this area of cardiovascular research.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Kidney Disease
Keywords
Chronic Kidney Failure, Vascular Calcification, Bisphosphonates

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare Provider
Allocation
Randomized
Enrollment
25 (Actual)

8. Arms, Groups, and Interventions

Arm Title
1
Arm Type
Active Comparator
Arm Description
Arm #1 will include patients randomized to receive bisphosphonate therapy for 24 months.
Arm Title
2
Arm Type
Placebo Comparator
Arm Description
Arm #2 will include patients randomized to receive placebo therapy for 24 months
Intervention Type
Drug
Intervention Name(s)
Bisphosphonate
Other Intervention Name(s)
Residronate
Intervention Description
35mg given orally once weekly for 24 months
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
identical placebo pill once weekly for 24 months
Primary Outcome Measure Information:
Title
Absolute change in coronary artery calcification score (CaSc) from baseline to study completion.
Time Frame
24 months
Secondary Outcome Measure Information:
Title
Change in bone density score (wrist/hip) as calculated by Ct scanning method, # fractures, MI, Stroke, amputation/surgery for peripheral revascularization.
Time Frame
24 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: 18 years of age receiving maintenance renal replacement therapy for less than 12 months incident patients starting renal replacement therapy for the first time Exclusion Criteria: active vasculitis severe hypocalcemia previous adverse side effect to bisphosphonate use current use of corticosteroids weight greater than 300 pounds pregnancy not expected to survive greater than one year expected to discontinue renal replacement therapy during the study period or recover renal function evidence of adynamic bone disease current bisphosphonate use
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Karen E Yeates, Dr
Organizational Affiliation
Queen's University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Kingston General Hospital
City
Kingston
State/Province
Ontario
ZIP/Postal Code
K7L 2V7
Country
Canada

12. IPD Sharing Statement

Learn more about this trial

Queen's University Investigation of Calcification in Chronic Kidney Disease

We'll reach out to this number within 24 hrs