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Effect of Dietary Sodium and Potassium Citrate on Renal Mineral Handling

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The University of Chicago

Status

Terminated

Conditions

Kidney Stone

Treatments

Dietary Supplement: Sodium and Potassium Citrate
Dietary Supplement: Placebo

Study type

Interventional

Funder types

Other

Identifiers

NCT03281928
IRB17-0992

Details and patient eligibility

About

This study intends to characterize the affect of sodium and potassium citrate in the diet on renal function.

Enrollment

30 patients

Sex

All

Ages

18 to 70 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • age 18 - 70, approximately equal numbers of men and women
  • studied by endoscopy with complete papillary mapping and grading
  • stone formers

Exclusion criteria

  • Patients with primary renal diseases or renal impairment (eGFR < 90), or medical conditions such as diabetes, or systemic diseases or medications that alter calcium metabolism
  • Patients with known bladder voiding problems

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Double Blind

30 participants in 4 patient groups, including a placebo group

Low Sodium plus Potassium Citrate
Experimental group
Treatment:
Dietary Supplement: Sodium and Potassium Citrate
Low Sodium plus placebo
Placebo Comparator group
Treatment:
Dietary Supplement: Placebo
High Sodium plus Potassium Citrate
Experimental group
Treatment:
Dietary Supplement: Sodium and Potassium Citrate
High Sodium plus placebo
Placebo Comparator group
Treatment:
Dietary Supplement: Placebo

Trial contacts and locations

1

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Central trial contact

Elaine Worcester

Data sourced from clinicaltrials.gov

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