Phase
Condition
N/ATreatment
Potassium citrate + crystal light
Crystal light
Potassium citrate
Clinical Study ID
Ages 18-80 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Men and women between age 18-80 years
Willing to follow experimental protocol
Willing to complete 24-hour urine collections (three total)
Willing to sign the informed consent form
Completed Litholink Collection with blood work with results a. hypocitraturia OR aciduria i. Hypocitraturics must meet definition of < 450mg/day for men < 550 mg/day for women. b. Low urine pH must be less than 5.6 c. potassium, BUN, creatinine, eGFR andhemoglobin A1c within normal limits
Exclusion
Exclusion Criteria:
Patients with severe hypocitraturia < 200 mg/day (men or women)
Patients with hyperkalemia, uncontrolled diabetes, chronic kidney disease, adrenalinsufficiency, delayed gastric emptying (or drug induced delayed gastric emptying),peptic ulcer disease, or active UTI
Patients with distal renal tubular acidosis or medication induced RTA (e.g. carbonicanhydrase inhibitor, topiramate)
Members of vulnerable patient populations
Allergies to ingredients in crystal light
Patients lacking decisional capacity
Study Design
Connect with a study center
Northwestern University
Chicago, Illinois 60611
United StatesActive - Recruiting
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