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Completed

NCT Number: NCT07162974

Litholytic Therapy for Coral Urate Nephrolithiasis

This is a prospective cohort study, patients with coralloid nephrolithiasis. Purpose of the study: to evaluate the efficacy and safety of litholytic therapy of coral-like urate nephrolithiasis with citrate mixtures.

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Key information

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Moscow state university of medicine and dentistry named after A.I. Evdokimov

Moscow, 127473, Russia

About this study

Anthropometric parameters height and weight were recorded in all patients, body mass index was calculated. All patients underwent MSCT of the urinary tract to assess the volume of density and concrements before the start of therapy. Biochemical blood analysis included determination of creatinine level with subsequent calculation of SCF. Urine pH was monitored for 72 hours using an electronic pH meter before therapy and recorded in a diary by patients three times a day, after which the average pH was calculated. Patients who met the inclusion criteria were included in the study after signing informed consent.

Who can participate

Healthy volunteers accepted: Yes

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

  • Coral-shaped calculus, which fills one or more calyx and pelvis (K2-K4 according to the classification of coral-shaped concretions);
  • The urate composition of the kidney stone was confirmed using dual-energy MSCT;
  • Unimpaired or restored (by draining the kidney) urine outflow from the kidney;
  • Persistently acidic urine pH (pH 5.8 or less);
  • Stone density is 550 Hounsfield units or less;
  • Informed voluntary consent of the patient to participate in the study;
  • Patient's readiness for conservative treatment;
  • No contraindications to therapy with citrate mixtures;

Treatment and study plan

anhydrous citric acid - 1197.0 mg, potassium bicarbonate - 967.5 mg, sodium citrate anhydrous - 835.5 mg

Drug

The dosage was selected individually for each patient, the target pH was considered to be 7.2

Primary outcomes

  1. Assessment of the size, volume and density of stones.

    Time frame: 1 month

    Computer tomography is the "gold standard" for diagnosing urolithiasis; it will allow you to identify stones, determine their size, density, structure, location, and assess the condition of the urinary tract.

Secondary outcomes

  1. Kidney function

    Time frame: 1 month

    Glomerular filtration rate (GFR, ml/min/1.73 m2) is a test used to check how well the kidneys are working. Specifically, it estimates how much blood passes through the glomeruli each minute. A GFR of 60 or higher is in the normal range. A GFR below 60 may mean kidney disease. A GFR of 15 or lower may mean kidney failure.

    The measurement of the glomerular filtration rate will be measured according to the results of the blood test

  2. Assessing the composition of stones

    Time frame: 6 months

    Chemical analysis of stones is a spectrometric (infrared spectroscopy) method that determines its exact composition by analyzing how the stone absorbs infrared radiation. Chemical analysis of stones will be performed on those patients who will undergo surgical treatment.

Sponsors and collaborators

Lead sponsor

Moscow State University of Medicine and Dentistry

Other

Registry information

Important dates

Study start
2023
Primary completion
2024
Study completion
2025
First posted
Sep 9, 2025
Registry last updated
Sep 9, 2025

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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