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Completed

NCT Number: NCT05365477

Empiric Versus Selective Prevention Strategies for Kidney Stone Disease

The aims of this study are to 1) Conduct a randomized clinical trial of selective versus empiric diet plus pharmacologic therapy in high-risk stone formers and 2) Determine adverse effects from, and adherence to selective and empiric strategies.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

Vanderbilt University Medical Center

Nashville, Tennessee, 37232, United States

About this study

Diet and pharmacologic interventions for preventing future kidney stone episodes are effective, however clinical guideline panels disagree on whether clinicians should perform selective therapy: performing 24-hour urine testing to guide choosing interventions to correct abnormal urinary parameters. The alternative strategy is empiric therapy: applying interventions without 24-hour urine testing. While 24-hour urine testing is considered the standard of care by nephrology and urology specialties for higher risk patients, the American College of Physicians does not recommend 24-hour urine testing.

This is a randomized clinical trial of selective versus empiric therapy for patients with presumed idiopathic calcium stone disease, representing >80% of the kidney stone population. The primary outcome is change in urinary supersaturation, which associates with symptomatic stone recurrence. We will recruit patients with presumed idiopathic calcium stone disease with at least 2 stone events within the previous 5 years. Participants will be randomly assigned to empiric diet plus thiazide with potassium citrate daily, or to selective diet plus pharmacologic therapy based on the 24-hour urine abnormalities identified at baseline and adjusted during follow-up. The primary outcomes will be the calculated calcium oxalate and calcium phosphate supersaturations. In addition, we will determine adverse effects from, and adherence to, selective and empiric strategies.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Two or more symptomatic kidney stone events in the last 5 years
  • Adult

Exclusion criteria

  • Medullary sponge kidney or renal tubular acidosis
  • Untreated urinary obstruction
  • Primary hyperparathyroidism
  • Primary hyperoxaluria
  • Pregnancy
  • Inflammatory bowel disease or bowel resection
  • Sarcoidosis
  • Cystinuria
  • Prior stone composition with uric acid, struvite, cystine, carbonate apatite
  • Use of specific medications (thiazides, topiramate, xanthine oxidase inhibitors, citrate, bicarbonate)
  • Chronic kidney disease stage 3 or higher (eGFR<60)
  • Gouty arthritis or 3 gout episodes in 1 year
  • Known allergy to study medications
  • Hypokalemia or hyponatremia at screening.
  • Age < 18 years

Treatment and study plan

Empiric Therapy: Diet

Behavioral

Diet: High water intake - at least 2.5 liters daily Reduce sugar-sweetened cola intake to ≤3 cans per week. Reduce salt intake to <2000mg sodium daily Reduce red meat intake to two 4-ounce portions per week Normal calcium intake: 3 servings of dairy products (or their equivalents) per day Increase vegetable and fruit intake to ≥5 servings per day Reduce oxalate intake to <100 mg/day

Empiric Therapy: Drug

Drug

Drug(s): indapamide 1.25mg and potassium citrate 15mEq daily.

Selective Therapy: Diet

Behavioral

Diet:

Volume <2.5L Increase fluid intake to ≥ 2.5L/d, based on specific urine volume

Calcium >250mg male, >200mg female Reduce red meat intake to two 4-oz portions/wk; reduce sodium intake to<2000mg/d, avoid vitamin D + calcium supplements

Oxalate >40mg Reduce dietary oxalate intake to <100 mg/d; increase fiber intake to 25-35 g/d

Citrate <450mg male, <550mg female Reduce red meat intake to two 4-oz portions/wk; increase fruit and vegetable intake to ≥5 svgs/d

pH<5.8 Reduce red meat intake to two 4-oz portions/wk; increase fruit and vegetable intake to ≥5 svgs/d

Uric acid >800mg male, >750mg female Reduce red meat intake to two 4- oz portions/wk; increase fruit and vegetable intake to ≥5 svgs/d

Sodium >150mmol Reduce sodium intake to <2000mg/d

Sulfate > 80mEq or urine urea nitrogen >14g Reduce red meat intake to three 3-4 oz portions/wk; increase fruit and vegetable intake to ≥5 svgs/d

Selective Therapy: Drug

Drug

Drug(s):

For calcium >250mg male, >200mg female: indapamide 1.25mg and potassium chloride 20mEq. At 1 month if persistent, then increase to indapamide 2.5mg and potassium chloride 20mEq. For citrate <450mg male, <550mg female: potassium citrate 15mEq BID. At 1 month if persistent, then increase to potassium citrate 30mEq BID. For pH<5.8: potassium citrate 15mEq BID. At month if persistent, then increase to potassium citrate 30mEq BID. For uric acid >800mg male, >750mg female: allopurinol 300mg.

If both elevated calcium and low pH: indapamide 1.25mg and potassium citrate 15mEq BID If both elevated calcium and low citrate: indapamide 1.25mg and potassium citrate 15mEq BID

Primary outcomes

  1. Calcium oxalate supersaturation

    Time frame: Baseline compared to two months

    Calculated calcium oxalate supersaturation in urine

  2. Calcium phosphate supersaturation

    Time frame: Baseline compared to two months

    Calculated calcium phosphate supersaturation in urine

Secondary outcomes

  1. Uric acid supersaturation

    Time frame: Baseline compared to two months

    Calculated uric acid supersaturation in urine

  2. 24hr urine parameters

    Time frame: Baseline compared to two months

    Urinary volume, calcium, oxalate, potassium, citrate, pH, uric acid, and sodium

Other outcomes

  1. 24hr urine parameters from baseline to month 1

    Time frame: Baseline to 1 month

    Calculated urinary supersaturations of calcium oxalate, calcium phosphate, uric acid, and urinary volume, calcium, oxalate, potassium, citrate, pH, uric acid, and sodium

  2. 24hr urine parameters from month 1 to month 2

    Time frame: 1 month to 2 months

    Calculated urinary supersaturations of calcium oxalate, calcium phosphate, uric acid, and urinary volume, calcium, oxalate, potassium, citrate, pH, uric acid, and sodium

  3. Kidney stone events

    Time frame: Baseline to 2 months

    Assessment of short term kidney stone events by self report and clinical imaging, if available

  4. Adverse events

    Time frame: Baseline to 2 months

    Assessment of adverse events - subjective and new hypokalemia, hyponatremia, hypomagnesemia, gouty arthritis or requiring uric acid lowering therapy, newly developed overt diabetes mellitus, allergic reactions, abnormal heart rate and blood pressure.

  5. Diet adherence

    Time frame: Baseline to 2 months

    Food diaries

  6. Medication adherence

    Time frame: Baseline to 2 months

    Pill counts

Sponsors and collaborators

Lead sponsor

Vanderbilt University Medical Center

Other

Registry information

Official study title

Randomized Trial of Empiric Versus Selective Prevention Strategies for Kidney Stone Disease

Important dates

Study start
2022
Primary completion
2025
Study completion
2026
First posted
May 9, 2022
Registry last updated
Jun 3, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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