Potassium Citrate and Crystal Light Lemonade
- Conditions
- Kidney Stone
- Interventions
- Registration Number
- NCT05389995
- Lead Sponsor
- Northwestern University
- Brief Summary
To define the effect of crystal light, potassium citrate, or both on urinary stone risk factors in patients with a history of stone and hypocitraturia/low pH
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- All
- Target Recruitment
- 10
-
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 < 450 mg/day for men < 550 mg/day for women.
b. Low urine pH must be less than 5.6 c. potassium, BUN, creatinine, eGFR and hemoglobin A1c within normal limits
- Patients with severe hypocitraturia < 200 mg/day (men or women)
- Patients with hyperkalemia, uncontrolled diabetes, chronic kidney disease, adrenal insufficiency, 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. carbonic anhydrase inhibitor, topiramate)
- Members of vulnerable patient populations
- Allergies to ingredients in crystal light
- Patients lacking decisional capacity
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- CROSSOVER
- Arm && Interventions
Group Intervention Description Crystal light Crystal light - Crystal light + potassium citrate Potassium citrate + crystal light - Potassium citrate Potassium citrate -
- Primary Outcome Measures
Name Time Method urine citrate levels Day 7 of week 5 24 hour urine collection
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Northwestern University
🇺🇸Chicago, Illinois, United States