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Comparing Alkalinizing Agents Efficacy on Stone Risk in Patients on a Metabolically Controlled Diet

Primary Purpose

Kidney Stone

Status
Recruiting
Phase
Early Phase 1
Locations
United States
Study Type
Interventional
Intervention
Potassium citrate
Sodium bicarbonate
Litholyte
Crystal Lite
Potassium Bicarbonate
Sponsored by
University of Texas Southwestern Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Kidney Stone

Eligibility Criteria

18 Years - 90 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Adults aged 18 and older.
  • with or without a history of stone disease.

Exclusion Criteria:

  • They are unable to take any of the medications due to health reasons.
  • Participants are pregnant or nursing.
  • Participants are unable to adhere to the metabolic diet.
  • Participants had a prior adverse event from one or more of the medications.

Sites / Locations

  • University of Texas Southwestern Medical CenterRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm 5

Arm 6

Arm Type

Placebo Comparator

Active Comparator

Active Comparator

Active Comparator

Active Comparator

Active Comparator

Arm Label

Metabolic diet

Potassium citrate

Sodium Bicarbonate

Litholyte arm

Crystal Lite

Potassium Bicarbonate

Arm Description

Controlled metabolic diet arm.

Outcomes

Primary Outcome Measures

24 hour urine volume
Total urine volume
24 hour urine volume
Total urine volume
24 hour urine creatinine
Urine creatinine
24 hour urine creatinine
Urine creatinine
24 hour urine calcium
urine calcium
24 hour urine calcium
urine calcium
24 hour urine potassium
Urine potassium
24 hour urine potassium
Urine potassium
24 hour urine sodium
Urine sodium
24 hours urine sodium
Urine sodium
24 hours urine citrate
Urine citrate
24 hours urine citrate
Urine citrate
24 hours urine uric acid
Urine uric acid
24 hours urine uric acid
Urine Uric Acid
24 hours urine oxalate
Urine oxalate
24 hours urine oxalate
Urine oxalate
24 hours urine magnesium
Urine magnesium
24 hours urine magnesium
Urine magnesium
24 hours urine ammonia
Urine ammonia
24 hours urine ammonia
Urine ammonia
24 Hour Urine pH
Overal Urine pH from 24h urine sample.
24 Hour Urine pH
Overal Urine pH from 24h urine sample.
24 hour urine phosphorus
Urine phosphorus
24 hour urine phosphorus
Urine phosphorus
24 hour urine sulfate
Urine sulfate
24 hour urine sulfate
Urine sulfate

Secondary Outcome Measures

# of patient who adherence to 100% Medication
Patient's adherence to medication for duration of study.
Total out of pocket cost
Calculate and compare treatment costs for the different interventions (in American dollars).
Patient's Satisfaction Survey
Patient satisfaction survey, adapted from the Treatment Satisfaction Questionnaire for Medication-14. Patients are queried on their satisfaction, with 9 questions for each medication.
Patient's GI Distress
Patient's GI distress symptom scale measures patients GI distress. There are 18 questions with descriptive answers ranging from "none", "mild", "moderate", "quite a lot" and "unbearable". There are no numerical scores, rather just descriptive scores. "None" means no GI distress, "unbearable" means that you are in a lot of distress from your GI symptoms.

Full Information

First Posted
November 4, 2020
Last Updated
August 17, 2023
Sponsor
University of Texas Southwestern Medical Center
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1. Study Identification

Unique Protocol Identification Number
NCT04651088
Brief Title
Comparing Alkalinizing Agents Efficacy on Stone Risk in Patients on a Metabolically Controlled Diet
Official Title
Evaluation of Multiple Alkalinizing Agents on Urinary Stone Risk Parameters in Stone and Non-stone Formers on a Metabolically Controlled Diet
Study Type
Interventional

2. Study Status

Record Verification Date
August 2023
Overall Recruitment Status
Recruiting
Study Start Date
March 16, 2021 (Actual)
Primary Completion Date
January 15, 2024 (Anticipated)
Study Completion Date
January 15, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Texas Southwestern Medical Center

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
Yes

5. Study Description

Brief Summary
The purpose of this study is to compare over the counter and alternative prescription urinary alkalinizing agents to slow release potassium citrate in their ability to modify urinary parameters associated with stone formation.
Detailed Description
Kidney stones are a common medical problem, occurring in almost 10% of people in the United States1. Furthermore, 50% of patients will recur within 10 years2. Metabolic testing is advised in recurrent stone formers, as well as those considered high risk, to assess for a specific abnormality which may prompt intervention to prevent future stone formation. Non-surgical interventions include both dietary counselling, as well as pharmacotherapy. One of the most commonly prescribed class of pharmacotherapies is alkali therapy which can be used to both increase the urinary pH and raise the urine citrate levels. This is particularly useful as correction of very acidic urinary pH (<5.5) can counteract uric acid crystallization thereby preventing or even dissolving uric acid stones3. Further, citrate has been shown to be a potent inhibitor of calcium stones by binding to the calcium directly4 and inhibiting crystal nucleation, thereby reducing calcium stone formation5,6. The most commonly utilized preparation of alkali therapy is potassium citrate which has been shown to prevent stone formation better than sodium citrate7. Unfortunately, some forms of potassium citrate (crystal packets) have become unavailable, and the slow release form of potassium citrate (UroCit-K) now exceeds $15/day in cost8. There have been multiple alternative alkali therapies that have been used in place of potassium citrate, including both medical foods and prescription medications, but with little evidence to support their use. A pilot study in order to quantify the metabolic effects of these agents and compare them to potassium citrate will be performed.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Kidney Stone

7. Study Design

Primary Purpose
Prevention
Study Phase
Early Phase 1
Interventional Study Model
Parallel Assignment
Masking
InvestigatorOutcomes Assessor
Allocation
Non-Randomized
Enrollment
15 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Metabolic diet
Arm Type
Placebo Comparator
Arm Description
Controlled metabolic diet arm.
Arm Title
Potassium citrate
Arm Type
Active Comparator
Arm Title
Sodium Bicarbonate
Arm Type
Active Comparator
Arm Title
Litholyte arm
Arm Type
Active Comparator
Arm Title
Crystal Lite
Arm Type
Active Comparator
Arm Title
Potassium Bicarbonate
Arm Type
Active Comparator
Intervention Type
Drug
Intervention Name(s)
Potassium citrate
Intervention Description
Slow release potassium citrate UroCit-K. Participants will take 20mEq twice daily.
Intervention Type
Drug
Intervention Name(s)
Sodium bicarbonate
Intervention Description
650mg tabs. Take 3 tabs twice daily.
Intervention Type
Dietary Supplement
Intervention Name(s)
Litholyte
Intervention Description
One packet is taken with 170ml of water. Two packets daily.
Intervention Type
Dietary Supplement
Intervention Name(s)
Crystal Lite
Intervention Description
The classic lemonade contains 21.7mEq/liter of alkali Therefore, patients will take 2 litres daily to have the 40mEq of alkali daily needed.
Intervention Type
Drug
Intervention Name(s)
Potassium Bicarbonate
Intervention Description
20 mEq tablets, one tablet twice daily
Primary Outcome Measure Information:
Title
24 hour urine volume
Description
Total urine volume
Time Frame
Change from baseline (Day 4) to initial start on treatment (Day 5)
Title
24 hour urine volume
Description
Total urine volume
Time Frame
Change from baseline (Day 4) to end of study (day 12)
Title
24 hour urine creatinine
Description
Urine creatinine
Time Frame
Change from baseline (Day 4) to initial start on treatment (Day 5)
Title
24 hour urine creatinine
Description
Urine creatinine
Time Frame
Change from baseline (Day 4) to end of study (day 12)
Title
24 hour urine calcium
Description
urine calcium
Time Frame
Change from baseline (Day 4) to initial start on treatment (Day 5)
Title
24 hour urine calcium
Description
urine calcium
Time Frame
Change from baseline (Day 4) to end of study (day 12)
Title
24 hour urine potassium
Description
Urine potassium
Time Frame
Change from baseline (Day 4) to initial start on treatment (Day 5)
Title
24 hour urine potassium
Description
Urine potassium
Time Frame
Change from baseline (Day 4) to end of study (day 12)
Title
24 hour urine sodium
Description
Urine sodium
Time Frame
Change from baseline (Day 4) to initial start on treatment (Day 5)
Title
24 hours urine sodium
Description
Urine sodium
Time Frame
Change from baseline (Day 4) to end of study (day 12)
Title
24 hours urine citrate
Description
Urine citrate
Time Frame
Change from baseline (Day 4) to initial start on treatment (Day 5)
Title
24 hours urine citrate
Description
Urine citrate
Time Frame
Change from baseline (Day 4) to end of study (day 12)
Title
24 hours urine uric acid
Description
Urine uric acid
Time Frame
Change from baseline (Day 4) to initial start on treatment (Day 5)
Title
24 hours urine uric acid
Description
Urine Uric Acid
Time Frame
Change from baseline (Day 4) to end of study (day 12)
Title
24 hours urine oxalate
Description
Urine oxalate
Time Frame
Change from baseline (Day 4) to initial start on treatment (Day 5)
Title
24 hours urine oxalate
Description
Urine oxalate
Time Frame
Change from baseline (Day 4) to end of study (day 12)
Title
24 hours urine magnesium
Description
Urine magnesium
Time Frame
Change from baseline (Day 4) to initial start on treatment (Day 5)
Title
24 hours urine magnesium
Description
Urine magnesium
Time Frame
Change from baseline (Day 4) to end of study (day 12)
Title
24 hours urine ammonia
Description
Urine ammonia
Time Frame
Change from baseline (Day 4) to initial start on treatment (Day 5)
Title
24 hours urine ammonia
Description
Urine ammonia
Time Frame
Change from baseline (Day 4) to end of study (day 12)
Title
24 Hour Urine pH
Description
Overal Urine pH from 24h urine sample.
Time Frame
Change from baseline (Day 4) to initial start on treatment (Day 5)
Title
24 Hour Urine pH
Description
Overal Urine pH from 24h urine sample.
Time Frame
Change from baseline (Day 4) to end of study (day 12)
Title
24 hour urine phosphorus
Description
Urine phosphorus
Time Frame
Change from baseline (Day 4) to initial start on treatment (Day 5)
Title
24 hour urine phosphorus
Description
Urine phosphorus
Time Frame
Change from baseline (Day 4) to end of study (day 12)
Title
24 hour urine sulfate
Description
Urine sulfate
Time Frame
Change from baseline (Day 4) to initial start on treatment (Day 5)
Title
24 hour urine sulfate
Description
Urine sulfate
Time Frame
Change from baseline (Day 4) to end of study (day 12)
Secondary Outcome Measure Information:
Title
# of patient who adherence to 100% Medication
Description
Patient's adherence to medication for duration of study.
Time Frame
At the end of study approximately 10 weeks after start of study.
Title
Total out of pocket cost
Description
Calculate and compare treatment costs for the different interventions (in American dollars).
Time Frame
At the end of study approximately 10 weeks after start of study.
Title
Patient's Satisfaction Survey
Description
Patient satisfaction survey, adapted from the Treatment Satisfaction Questionnaire for Medication-14. Patients are queried on their satisfaction, with 9 questions for each medication.
Time Frame
At the end of study approximately 10 weeks after start of study.
Title
Patient's GI Distress
Description
Patient's GI distress symptom scale measures patients GI distress. There are 18 questions with descriptive answers ranging from "none", "mild", "moderate", "quite a lot" and "unbearable". There are no numerical scores, rather just descriptive scores. "None" means no GI distress, "unbearable" means that you are in a lot of distress from your GI symptoms.
Time Frame
At the end of study approximately 10 weeks after start of study.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
90 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Adults aged 18 and older. with or without a history of stone disease. Exclusion Criteria: They are unable to take any of the medications due to health reasons. Participants are pregnant or nursing. Participants are unable to adhere to the metabolic diet. Participants had a prior adverse event from one or more of the medications.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Margaret Pearle
Phone
214-648-6853
Email
margaret.pearle@utsouthwestern.edu
First Name & Middle Initial & Last Name or Official Title & Degree
Jessica Dai
Email
jessica.dai@utsouthwestern.edu
Facility Information:
Facility Name
University of Texas Southwestern Medical Center
City
Dallas
State/Province
Texas
ZIP/Postal Code
75390
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Margaret Pearle
Phone
214-648-6853
Email
margaret.pearle@utsouthwestern.edu

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
22498635
Citation
Scales CD Jr, Smith AC, Hanley JM, Saigal CS; Urologic Diseases in America Project. Prevalence of kidney stones in the United States. Eur Urol. 2012 Jul;62(1):160-5. doi: 10.1016/j.eururo.2012.03.052. Epub 2012 Mar 31.
Results Reference
background
PubMed Identifier
2688503
Citation
Uribarri J, Oh MS, Carroll HJ. The first kidney stone. Ann Intern Med. 1989 Dec 15;111(12):1006-9. doi: 10.7326/0003-4819-111-12-1006.
Results Reference
background
PubMed Identifier
24857648
Citation
Pearle MS, Goldfarb DS, Assimos DG, Curhan G, Denu-Ciocca CJ, Matlaga BR, Monga M, Penniston KL, Preminger GM, Turk TM, White JR; American Urological Assocation. Medical management of kidney stones: AUA guideline. J Urol. 2014 Aug;192(2):316-24. doi: 10.1016/j.juro.2014.05.006. Epub 2014 May 20.
Results Reference
background
PubMed Identifier
3784284
Citation
Pak CY, Sakhaee K, Fuller C. Successful management of uric acid nephrolithiasis with potassium citrate. Kidney Int. 1986 Sep;30(3):422-8. doi: 10.1038/ki.1986.201.
Results Reference
background
PubMed Identifier
9228722
Citation
Ryall RL. Urinary inhibitors of calcium oxalate crystallization and their potential role in stone formation. World J Urol. 1997;15(3):155-64. doi: 10.1007/BF02201852. No abstract available.
Results Reference
background
PubMed Identifier
4009822
Citation
Preminger GM, Sakhaee K, Skurla C, Pak CY. Prevention of recurrent calcium stone formation with potassium citrate therapy in patients with distal renal tubular acidosis. J Urol. 1985 Jul;134(1):20-3. doi: 10.1016/s0022-5347(17)46963-1.
Results Reference
background
PubMed Identifier
9366314
Citation
Ettinger B, Pak CY, Citron JT, Thomas C, Adams-Huet B, Vangessel A. Potassium-magnesium citrate is an effective prophylaxis against recurrent calcium oxalate nephrolithiasis. J Urol. 1997 Dec;158(6):2069-73. doi: 10.1016/s0022-5347(01)68155-2.
Results Reference
background
PubMed Identifier
3339718
Citation
Preminger GM, Sakhaee K, Pak CY. Alkali action on the urinary crystallization of calcium salts: contrasting responses to sodium citrate and potassium citrate. J Urol. 1988 Feb;139(2):240-2. doi: 10.1016/s0022-5347(17)42374-3.
Results Reference
background
PubMed Identifier
31333065
Citation
Stern KL, Canvasser N, Borofsky M, Gleason VM, Kamphuis G, El Tayeb MM, Hsi R, Scotland KB. Alkalinizing Agents: A Review of Prescription, Over-the-Counter, and Medical Food Supplements. J Endourol. 2020 Jan;34(1):1-6. doi: 10.1089/end.2019.0292. Epub 2019 Sep 25.
Results Reference
background

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Comparing Alkalinizing Agents Efficacy on Stone Risk in Patients on a Metabolically Controlled Diet

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