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Metabolic Acidosis in Renal Transplant Patients (MART)

Primary Purpose

Renal Transplant Patients, Metabolic Acidosis, Physical Capacity

Status
Completed
Phase
Phase 2
Locations
Switzerland
Study Type
Interventional
Intervention
Potassium citrate
Potassium chloride
Sponsored by
University of Zurich
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Renal Transplant Patients focused on measuring Renal transplantation, Metabolic acidosis, Physical capacity, Bone histology, Bone histomorphometry, Parathyroid function, Calcium and phosphate metabolism

Eligibility Criteria

20 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients with a renal graft having been transplanted within the previous 8 years and being at least 3 months post transplantation, or, patients scheduled to undergo transplantation from a living organ donor within the upcoming 3 months
  • Venous serum bicarbonate concentration < 24 mmol/L at time of baseline determination
  • Renal transplant function with a calculated glomerular filtration rate (GFR) greater or equal 30 ml/min according to the Cockcroft-Gault formula
  • Immunosuppressive therapy including a calcineurin inhibitor (cyclosporine A or tacrolimus)
  • Age 20 through 65 years of either sex
  • Written informed consent for study participation

Exclusion Criteria:

  • Acute rejection episode requiring specific therapy within 4 weeks before study inclusion
  • Severe impairment in general health and/or physical handicaps (malignant neoplasia, catabolic state, acute systemic infection requiring therapy)
  • Mental illness, psychiatric disorder
  • Tetracycline intolerance
  • Planned or "overt" pregnancy

Sites / Locations

  • University Hospital of Zurich

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Postassium citrate

Potassium chloride

Arm Description

Aim: correction of metabolic acidosis

Potassium chloride is given to compensate for any possible effects of potassium in potassium citrate (primary treatment).

Outcomes

Primary Outcome Measures

Correction of metabolic acidosis

Secondary Outcome Measures

Improvement in physical capacity

Full Information

First Posted
April 1, 2009
Last Updated
October 21, 2010
Sponsor
University of Zurich
Collaborators
University of Texas Southwestern Medical Center, Swiss Federal Institute of Technology
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1. Study Identification

Unique Protocol Identification Number
NCT00913796
Brief Title
Metabolic Acidosis in Renal Transplant Patients
Acronym
MART
Official Title
Metabolic Acidosis and Its Impact on Mineral Metabolism and Physical Performance in Renal Transplant Patients
Study Type
Interventional

2. Study Status

Record Verification Date
June 2009
Overall Recruitment Status
Completed
Study Start Date
December 2007 (undefined)
Primary Completion Date
March 2010 (Actual)
Study Completion Date
March 2010 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
University of Zurich
Collaborators
University of Texas Southwestern Medical Center, Swiss Federal Institute of Technology

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Acidosis (accumulation of acid in the body) may be an underrecognized problem in patients after renal transplantation. It may have consequences on physical performance due to negative effects on bone and muscle metabolism. Therefore, the purpose of this study is to determine the status of physical capacity and bone structure in renal transplant patients with metabolic acidosis to study the effect of substituting base equivalents (citrate) on acid/base status of renal transplant patients with acidosis to compare the status of physical capacity and bone structure in renal transplant patients with metabolic acidosis before and after substitution with citrate
Detailed Description
Chronic kidney disease is developing to become one of the major health problems in the Western world with more than one million patients on renal replacement therapy, and many more expected in the years ahead [1]. Survival of patients with end stage renal disease has become possible with the introduction of dialysis therapy. Renal transplantation has resulted both in further reduction of mortality and improvement in quality of life for patients with end stage renal disease. Nevertheless, successful transplantation with regard to graft and patient survival is still associated with significant morbidity. Apart from infectious complications and cardiovascular disease, limitations in physical capacity from musculoskeletal disorders have become a relevant problem, resulting in reduced quality of life, poor physical functioning and inability to work. Muscle and bone metabolism in chronic kidney disease are typically disturbed resulting in significant pathology and dysfunction of the affected tissues. They are associated with metabolic disorders related to renal insufficiency, among which metabolic acidosis is a major contributor. Metabolic acidosis is a well recognized problem in renal transplant patients. However, its prevalence, pathogenesis, course and sequelae are not well established. In particular, its relation to post-transplant bone and muscle disorders, and the impact on physical capabilities in renal transplant patients have not been comprehensively investigated so far. The purpose of the proposed project is to examine the characteristics and pathogenesis of post-transplant metabolic acidosis, and its relation to bone and muscle pathologies and impact on physical capabilities in renal transplant patients. In particular, the following aims are proposed to investigate in de novo and long-term renal transplantation: Aim # 1: To examine the type, degree and course of metabolic acidosis in renal transplant patients, early and long-term after transplantation Aim # 2: To examine alterations in mineral and bone metabolism, and bone structure, and their relationship to the acid/base disorder Aim # 3: To examine overall physical performance, exercise capacity and muscle energy content, and their relationship to the acid/base disorder In order to analyze secondary effects of subclinical and overt acidosis on bone (Aim # 2) and muscle (Aim # 3), patients will be studied at baseline, and then be supplemented with base equivalents in order to achieve a stable plasma serum bicarbonate concentration of 24-26 mmol/l, and be reexamined thereafter. Completion of the three aims will allow to comprehensively analyze the pathogenesis of and interrelations between acid/base status, mineral metabolism, bone disorders and muscle function in renal transplant patients. This will be the first study to link metabolic alterations to structural and functional measures of the musculoskeletal system, and to the impact of the resulting pathologies on physical disabilities in patients with a kidney graft. We are in dire need to know the magnitude of the problem, whether to treat, and how aggressive to treat these patients. The results of this project will be indispensable regarding justification to rigorously evaluate and treat metabolic acidosis in patients with chronic renal insufficiency and after transplantation.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Renal Transplant Patients, Metabolic Acidosis, Physical Capacity, Bone Disease, Mineral Metabolism
Keywords
Renal transplantation, Metabolic acidosis, Physical capacity, Bone histology, Bone histomorphometry, Parathyroid function, Calcium and phosphate metabolism

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
30 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Postassium citrate
Arm Type
Experimental
Arm Description
Aim: correction of metabolic acidosis
Arm Title
Potassium chloride
Arm Type
Active Comparator
Arm Description
Potassium chloride is given to compensate for any possible effects of potassium in potassium citrate (primary treatment).
Intervention Type
Drug
Intervention Name(s)
Potassium citrate
Intervention Description
2.41 gram of citrate b.i.d. for 12 months. Dosage to be adjusted according to serum potassium concentration.
Intervention Type
Drug
Intervention Name(s)
Potassium chloride
Intervention Description
370 mg potassium t.i.d. for 12 months. Dosage to be adjusted according to serum postassium concentration.
Primary Outcome Measure Information:
Title
Correction of metabolic acidosis
Time Frame
12 months
Secondary Outcome Measure Information:
Title
Improvement in physical capacity
Time Frame
12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients with a renal graft having been transplanted within the previous 8 years and being at least 3 months post transplantation, or, patients scheduled to undergo transplantation from a living organ donor within the upcoming 3 months Venous serum bicarbonate concentration < 24 mmol/L at time of baseline determination Renal transplant function with a calculated glomerular filtration rate (GFR) greater or equal 30 ml/min according to the Cockcroft-Gault formula Immunosuppressive therapy including a calcineurin inhibitor (cyclosporine A or tacrolimus) Age 20 through 65 years of either sex Written informed consent for study participation Exclusion Criteria: Acute rejection episode requiring specific therapy within 4 weeks before study inclusion Severe impairment in general health and/or physical handicaps (malignant neoplasia, catabolic state, acute systemic infection requiring therapy) Mental illness, psychiatric disorder Tetracycline intolerance Planned or "overt" pregnancy
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Patrice M. Ambühl, M.D.
Organizational Affiliation
University of Zurich
Official's Role
Principal Investigator
Facility Information:
Facility Name
University Hospital of Zurich
City
Zurich
ZIP/Postal Code
CH 8091
Country
Switzerland

12. IPD Sharing Statement

Citations:
PubMed Identifier
22773591
Citation
Starke A, Corsenca A, Kohler T, Knubben J, Kraenzlin M, Uebelhart D, Wuthrich RP, von Rechenberg B, Muller R, Ambuhl PM. Correction of metabolic acidosis with potassium citrate in renal transplant patients and its effect on bone quality. Clin J Am Soc Nephrol. 2012 Sep;7(9):1461-72. doi: 10.2215/CJN.01100112. Epub 2012 Jul 5.
Results Reference
derived

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Metabolic Acidosis in Renal Transplant Patients

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