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Role Of Phosphorus And FGF 23 In Patients With Dent Disease

Primary Purpose

Dent Disease

Status
Completed
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
Phosphorus Supplement
Observation
Sponsored by
Mayo Clinic
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Dent Disease focused on measuring Dent, Dents, Dent Disease, Phosphorus Supplements, FGF 23

Eligibility Criteria

undefined - undefined (Child, Adult, Older Adult)MaleDoes not accept healthy volunteers

Inclusion Criteria:

Patients will be recruited from those in the RKSC Dent Registry

  1. Diagnostic criteria for Dent disease Observational arm include:

    1. <18 years old
    2. LMWP (at least 5 times above the upper limit of normal) and at least 1 of the following criteria: 1. Hypercalciuria, 2. Kidney stones, 3. Nephrocalcinosis, 4. Hypophosphatemia, 5. Renal phosphate leak, 6. Aminoaciduria, 7. Glucosuria without diabetes mellitus, 8. Hematuria, 9. Renal insufficiency, 10. Family history with x-linked inheritance or
    3. 1 of the above criteria (1-9) and confirmed genetic mutation of CLCN5 or OCRL1.
  2. Diagnostic criteria for Dent disease Intervention arm include:

    1. >18 years old
    2. LMWP (at least 5 times above the upper limit of normal) and at least 1 of the following criteria: 1. Hypercalciuria, 2. Kidney stones, 3. Nephrocalcinosis, 4. Hypophosphatemia, 5. Renal phosphate leak, 6. Aminoaciduria, 7. Glucosuria without diabetes mellitus, 8. Hematuria, 9. Renal insufficiency, 10. Family history with x-linked inheritance or
    3. 1 of the above criteria (1-9) and confirmed genetic mutation of CLCN5 or OCRL1.
  3. Idiopathic calcium nephrolithiasis with renal phosphate leak

    1. Male patients > 18 years old
    2. History of symptomatic calcium oxalate or calcium phosphate stone, hypercalciuria (>250 mg/24 hrs), renal phosphate leak (TMP/GFR <2.07 mg/dl)
  4. Idiopathic calcium nephrolithiasis without renal phosphate leak

    1. Male patients > 18 years old
    2. History of symptomatic calcium oxalate or calcium phosphate stone, hypercalciuria (>250 mg/24 hrs), renal phosphate leak (TMP/GFR <2.07 mg/dl)

Exclusion Criteria:

  1. Exclusion for Dent disease include: primary or secondary hyperparathyroidism, hyperthyroidism, chronic diarrhea states; intake of thiazide diuretics, glucocorticoids, or estrogens within one month of the study.
  2. Exclusion criteria for calcium stone formers include: primary or secondary hyperparathyroidism, hyperthyroidism, estimated GFR <40 ml/mn/1.73m2, chronic diarrhea states; intake of thiazide diuretics, glucocorticoids, or estrogens within one month of the study.
  3. Exclusion criteria include history of symptomatic or asymptomatic kidney stone disease; primary or secondary hyperparathyroidism; estimated GFR <40 ml/min/1.73m2, chronic diarrhea states; intake of thiazide diuretics, glucocorticoids, or estrogens within one month of the study.

Sites / Locations

  • Mayo Clinic

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Experimental

Placebo Comparator

Arm Label

Dent Disease Intervention

Kidney Stone subjects

Dent Disease Observation

Arm Description

Dent Disease subjects will receive 2 week supplementation with phosphorus

Kidney stone with or without phosphate leak subjects will receive 2 week supplementation with phosphorus

Dent disease subjects will not get phosphorus

Outcomes

Primary Outcome Measures

Change in Urine Total Protein
Urine protein tests detect and/or measure protein being released into the urine. Normal urine protein elimination is less than 150 mg/day

Secondary Outcome Measures

Full Information

First Posted
December 6, 2013
Last Updated
March 19, 2020
Sponsor
Mayo Clinic
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1. Study Identification

Unique Protocol Identification Number
NCT02016235
Brief Title
Role Of Phosphorus And FGF 23 In Patients With Dent Disease
Official Title
Role Of Phosphorus And FGF 23 In Patients With Dent Disease
Study Type
Interventional

2. Study Status

Record Verification Date
March 2020
Overall Recruitment Status
Completed
Study Start Date
September 2014 (undefined)
Primary Completion Date
January 2019 (Actual)
Study Completion Date
January 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Mayo Clinic

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Patients with Dent disease have suppressed levels of FGF 23 which contributes to hypercalciuria, kidney stones, nephrocalcinosis and renal failure. Supplementation with phosphorus may reduce hypercalciuria.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Dent Disease
Keywords
Dent, Dents, Dent Disease, Phosphorus Supplements, FGF 23

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1, Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
30 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Dent Disease Intervention
Arm Type
Experimental
Arm Description
Dent Disease subjects will receive 2 week supplementation with phosphorus
Arm Title
Kidney Stone subjects
Arm Type
Experimental
Arm Description
Kidney stone with or without phosphate leak subjects will receive 2 week supplementation with phosphorus
Arm Title
Dent Disease Observation
Arm Type
Placebo Comparator
Arm Description
Dent disease subjects will not get phosphorus
Intervention Type
Drug
Intervention Name(s)
Phosphorus Supplement
Other Intervention Name(s)
K-phos neutral
Intervention Description
250 mg po qid
Intervention Type
Other
Intervention Name(s)
Observation
Intervention Description
Baseline blood and urine measurements only
Primary Outcome Measure Information:
Title
Change in Urine Total Protein
Description
Urine protein tests detect and/or measure protein being released into the urine. Normal urine protein elimination is less than 150 mg/day
Time Frame
baseline, day 7

10. Eligibility

Sex
Male
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients will be recruited from those in the RKSC Dent Registry Diagnostic criteria for Dent disease Observational arm include: <18 years old LMWP (at least 5 times above the upper limit of normal) and at least 1 of the following criteria: 1. Hypercalciuria, 2. Kidney stones, 3. Nephrocalcinosis, 4. Hypophosphatemia, 5. Renal phosphate leak, 6. Aminoaciduria, 7. Glucosuria without diabetes mellitus, 8. Hematuria, 9. Renal insufficiency, 10. Family history with x-linked inheritance or 1 of the above criteria (1-9) and confirmed genetic mutation of CLCN5 or OCRL1. Diagnostic criteria for Dent disease Intervention arm include: >18 years old LMWP (at least 5 times above the upper limit of normal) and at least 1 of the following criteria: 1. Hypercalciuria, 2. Kidney stones, 3. Nephrocalcinosis, 4. Hypophosphatemia, 5. Renal phosphate leak, 6. Aminoaciduria, 7. Glucosuria without diabetes mellitus, 8. Hematuria, 9. Renal insufficiency, 10. Family history with x-linked inheritance or 1 of the above criteria (1-9) and confirmed genetic mutation of CLCN5 or OCRL1. Idiopathic calcium nephrolithiasis with renal phosphate leak Male patients > 18 years old History of symptomatic calcium oxalate or calcium phosphate stone, hypercalciuria (>250 mg/24 hrs), renal phosphate leak (TMP/GFR <2.07 mg/dl) Idiopathic calcium nephrolithiasis without renal phosphate leak Male patients > 18 years old History of symptomatic calcium oxalate or calcium phosphate stone, hypercalciuria (>250 mg/24 hrs), renal phosphate leak (TMP/GFR <2.07 mg/dl) Exclusion Criteria: Exclusion for Dent disease include: primary or secondary hyperparathyroidism, hyperthyroidism, chronic diarrhea states; intake of thiazide diuretics, glucocorticoids, or estrogens within one month of the study. Exclusion criteria for calcium stone formers include: primary or secondary hyperparathyroidism, hyperthyroidism, estimated GFR <40 ml/mn/1.73m2, chronic diarrhea states; intake of thiazide diuretics, glucocorticoids, or estrogens within one month of the study. Exclusion criteria include history of symptomatic or asymptomatic kidney stone disease; primary or secondary hyperparathyroidism; estimated GFR <40 ml/min/1.73m2, chronic diarrhea states; intake of thiazide diuretics, glucocorticoids, or estrogens within one month of the study.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
John C Lieske, M.D.
Organizational Affiliation
Mayo Clinic
Official's Role
Principal Investigator
Facility Information:
Facility Name
Mayo Clinic
City
Rochester
State/Province
Minnesota
ZIP/Postal Code
55905
Country
United States

12. IPD Sharing Statement

Links:
URL
https://www.mayo.edu/research/clinical-trials.
Description
Mayo Clinic Clinical Trials

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Role Of Phosphorus And FGF 23 In Patients With Dent Disease

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