search
Back to results

Effect of Allopurinol on Markers of Mineral and Bone Metabolism

Primary Purpose

Chronic Kidney Diseases, Osteodystrophy, Uric Acid Concentration, Serum, Quantitative Trait Locus 7

Status
Active
Phase
Not Applicable
Locations
Brazil
Study Type
Interventional
Intervention
Allopurinol
Sponsored by
University of Sao Paulo General Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Chronic Kidney Diseases focused on measuring chronic kidney disease, allopurinol, mineral and bone metabolism, uric acid, vitamin D

Eligibility Criteria

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

Inclusion Criteria: stage 3, 4 or 5 CKD on conservative management - Exclusion Criteria: allergy to allopurinol current treatment with allopurinol Gout

Sites / Locations

  • Hospital das Clinicas HCFMUSP

Arms of the Study

Arm 1

Arm 2

Arm Type

Placebo Comparator

Active Comparator

Arm Label

Placebo

Allopurinol

Arm Description

pills exactly as the drug will be delivered to participants. Instructions will be made to take the pill once a day.

pills exactly as the placebo will be delivered to participants. Instructions will be made to take the pill once a day.

Outcomes

Primary Outcome Measures

1,25 dihydroxivitamin D
Increase in 1,25 dihydroxivitamin D
FGF-23
Reduction of FGF-23
Klotho
Increase in alpha Klotho

Secondary Outcome Measures

Full Information

First Posted
October 26, 2022
Last Updated
August 28, 2023
Sponsor
University of Sao Paulo General Hospital
search

1. Study Identification

Unique Protocol Identification Number
NCT05601271
Brief Title
Effect of Allopurinol on Markers of Mineral and Bone Metabolism
Official Title
Effect of Allopurinol on Markers of Mineral and Bone Metabolism in Patients in With Chronic Kidney Disease: a Randomized Double-blind Study
Study Type
Interventional

2. Study Status

Record Verification Date
August 2023
Overall Recruitment Status
Active, not recruiting
Study Start Date
March 1, 2021 (Actual)
Primary Completion Date
December 30, 2023 (Anticipated)
Study Completion Date
April 30, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Sao Paulo General Hospital

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Hyperuricemia is a common condition in patients with chronic kidney disease (CKD) in the glomerular filtration rate. Recently, it has been suggested that uric acid is related to a mineral and bone disease of CKD (CKD-MBD) since the high concentration of uric acid is associated with the harmful effect of vitamin D. The proof of concept of the association between acid uric acid and CKD-MBD is based on a prospective study (sample size 6) that observed, after 1 week of use of allopurinol, an increase in the concentration of 1,25(2D, a result independent of the concentration of calcium, phosphorus, 25(OH)D and PTH. An experimental study found that hyperuricemia could modify the expression of the 1α-hydroxylase enzyme, consequently reducing 1,25(OH). The current study aims to evaluate the action of allopurinol on CKD-MBD biomarkers (25(OH)-vitamin D, 1,25(OH)2D, FGF-23, PTH, calcium and phosphorus). We hypothesize that allopurinol can improve serum levels of 1,25(OH) 2D and PTH. This is a controlled, randomized, double-blind study, defined as a filtration rate < 60ml/1.73 m², according to the CKD-EPI equation. Inclusion criteria: patients with stages III, IV and V CKD who are not on dialysis with a serum level of 25(OH)-vitamin D >20 ng/ml. Exclusion criteria: Patients diagnosed with gout, undergoing treatment with allopurinol, patients already in use and drugs with sensitivity to the drug. Based on a previous study, we calculated a sample for 2 groups (placebo and drug) with pre and post-measurements (a total of 4). Considering a standard deviation of 4 and a difference of 7 in the treated group, 3 in the placebo group, and an alpha error of 5%, we calculated a sample of 25 patients in each arm.
Detailed Description
In this randomized double-blind study, patients receive allopurinol or a placebo for 3 months. Dependent variables: 25(OH)-vitamin D, 1,25(OH)2D, FGF-23, PTH, calcium and phosphorus Population: stage 3, 4 or 5 CKD on conservative management at the Nephrology Service of Hospital das Clinicas HCFMUSP, Sao Paulo, Brazil. The same physician will follow patients. Adverse effects will be recorded.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Kidney Diseases, Osteodystrophy, Uric Acid Concentration, Serum, Quantitative Trait Locus 7
Keywords
chronic kidney disease, allopurinol, mineral and bone metabolism, uric acid, vitamin D

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
ParticipantInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
50 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
pills exactly as the drug will be delivered to participants. Instructions will be made to take the pill once a day.
Arm Title
Allopurinol
Arm Type
Active Comparator
Arm Description
pills exactly as the placebo will be delivered to participants. Instructions will be made to take the pill once a day.
Intervention Type
Drug
Intervention Name(s)
Allopurinol
Intervention Description
Allopurinol 100 to 300 mg a day for 3 months
Primary Outcome Measure Information:
Title
1,25 dihydroxivitamin D
Description
Increase in 1,25 dihydroxivitamin D
Time Frame
3 months
Title
FGF-23
Description
Reduction of FGF-23
Time Frame
3 months
Title
Klotho
Description
Increase in alpha Klotho
Time Frame
3 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: stage 3, 4 or 5 CKD on conservative management - Exclusion Criteria: allergy to allopurinol current treatment with allopurinol Gout
Facility Information:
Facility Name
Hospital das Clinicas HCFMUSP
City
São Paulo
State/Province
SP
ZIP/Postal Code
05403000
Country
Brazil

12. IPD Sharing Statement

Plan to Share IPD
Undecided

Learn more about this trial

Effect of Allopurinol on Markers of Mineral and Bone Metabolism

We'll reach out to this number within 24 hrs