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Clinical Trials/NCT01225796
NCT01225796
Completed
Early Phase 1

Randomized Trial of Sodium Bicarbonate in Renal Transplant Recipients With Low-normal Serum Bicarbonate Levels

University of Utah1 site in 1 country29 target enrollmentNovember 2010

Overview

Phase
Early Phase 1
Intervention
Sodium bicarbonate
Conditions
Kidney Transplantation
Sponsor
University of Utah
Enrollment
29
Locations
1
Primary Endpoint
Urinary transforming growth factor-beta1
Status
Completed
Last Updated
10 years ago

Overview

Brief Summary

The purpose of this study is to compare the effect of sodium bicarbonate versus no sodium bicarbonate treatment on urinary ammonia levels and urinary transforming growth factor-beta1 (TGF-beta1) excretion in renal transplant patients with low-to-normal serum bicarbonate levels (20 - 28 mmol/L).

Detailed Description

Renal allograft survival ten years after transplant is only about 50%. In people with non-transplant chronic kidney disease (CKD), sodium bicarbonate treatment seems to delay progressive decline in kidney function in those with low serum bicarbonate levels (metabolic acidosis). This may be because sodium bicarbonate reduces renal ammonia production and hence fibrosis. Observational evidence suggests that people with CKD and low-normal serum bicarbonate levels might also benefit from sodium bicarbonate treatment. TGF-beta1 levels seem to be an important predictor of chronic allograft nephropathy, and alkalinizing agents may have an effect on TFG-beta1 excretion. Retrospective analysis of participants in the African American Study of Kidney Disease and Hypertension showed the lowest risk of CKD progression was among those having baseline serum bicarbonate levels in the range of 28-30 mmol/L. Recent studies in people with pre-transplant CKD have suggested that increasing low serum bicarbonate levels (\< 22 mmol/L) with alkalinizing agents such as sodium bicarbonate and sodium citrate may reduce CKD progression. Design: this is an open-label randomized study testing the effect of a six-month intervention with sodium bicarbonate 650 mg orally thrice daily versus no sodium bicarbonate treatment on renal ammonia excretion and urinary TGF-beta1. Visits will occur at baseline, 3 months, and 6 months. At each follow-up visit, the study coordinator or principal investigator will review a medical questionnaire with the participant and collect a sample of blood and urine for analysis of urinary TGF-beta1, metabolic panel, pH, urinary net acid excretion, urinary bicarbonate and urinary ammonia.

Registry
clinicaltrials.gov
Start Date
November 2010
End Date
November 2012
Last Updated
10 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Kalani Raphael

Principal Investigator

University of Utah

Eligibility Criteria

Inclusion Criteria

  • Renal transplant recipients
  • Age 21-75 years
  • Six months since the time of the most recent transplant
  • Serum bicarbonate 20-28mM on the two most recent serum measures with the last six months
  • Stable creatinine

Exclusion Criteria

  • Systolic blood pressure \> 140mmHg
  • Diastolic blood pressure \> 90mmHg
  • Known ejection fraction \<50%
  • Clinical diagnosis of heart failure
  • Use of \>3 antihypertensive agents
  • \> 1+ edema
  • Use of alkali in the preceding 3 months
  • History of noncompliance with clinic visits

Arms & Interventions

Sodium bicarbonate

This group will receive oral sodium bicarbonate 650mg three times daily for 6 months.

Intervention: Sodium bicarbonate

Outcomes

Primary Outcomes

Urinary transforming growth factor-beta1

Time Frame: 6 months

This is considered a surrogate marker of chronic allograft nephropathy (tubulointerstitial fibrosis).

Secondary Outcomes

  • urinary ammonia excretion(6 months)

Study Sites (1)

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