Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT06944223 · ClinicalTrials.gov registry record · NA

Oxalate and Citrate in Humans - Response to Citrate

A NA study of Healthy and Kidney Stone, sponsored by University of Chicago.

Recruiting
Registry status
NA
Development phase
24
Enrollment target
1
Study location

NCT06944223: Recruiting NA study of Healthy and Kidney Stone, sponsored by University of Chicago.

NCT06944223 is a NA study of Healthy and Kidney Stone that is actively recruiting participants, run by University of Chicago. The registered enrollment target is 24 participants, below the 647-participant average among 1,090 other Healthy trials with a reported enrollment target (96% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT06944223, a NA study of Healthy and Kidney Stone, is actively recruiting participants, sponsored by University of Chicago.

RECRUITING
Registry status
NA
Development phase
24 participants
Enrollment target
1
Study location

Study Summary

This is a single-center study that aims to learn more about how two compounds found in food, oxalate and citrate, interact in the body and may influence a person's chances of forming kidney stones. The study will examine changes in urinary oxalate and citrate levels after participants consume potassium citrate.

Primary Outcome

Urine oxalate will be measured or calculated at time points 0, 2-hours, 4-hours, and 6-hours after sodium oxalate consumption. We will compare change in urine citrate and fractional excretion of citrate by change in oxalate at each time period for all participants.

Conditions Studied

Interventions

  • OTHER Kidney stone formers
  • OTHER Control cohort

Study Locations (1)

Illinois

  • University of Chicago Medical Center - Chicago

Trial Details

FieldValue
Enrollment Target 24 participants
Start Date 2025-10-01
Est. Completion 2027-06-01
Phase NA
University of Chicago

796 total trials

What NCT06944223 shows while recruiting

NCT06944223 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 24 participants, a relatively small participant target, below the 647-participant average among 1,090 other Healthy trials with a reported enrollment target (96% lower).

The record links to 2 conditions, with Healthy appearing as the primary indexed condition, and to 2 interventions - of which Kidney stone formers is the first listed.

NCT06944223 reports a single indexed study location in Illinois.

Frequently Asked Questions

What is clinical trial NCT06944223 about?

NCT06944223 is a clinical study titled "Oxalate and Citrate in Humans - Response to Citrate". This is a single-center study that aims to learn more about how two compounds found in food, oxalate and citrate, interact in the body and may influence a person's chances of forming kidney stones. The study will examine changes in urinary oxalate and citrate levels after participants consume potass...

What is the current status of trial NCT06944223?

This trial is currently recruiting. It is a NA study. The enrollment target is 24 participants. The study started on 2025-10-01. Estimated completion is 2027-06-01.

What conditions does trial NCT06944223 study?

This clinical trial studies the following conditions: Healthy, Kidney Stone.

What interventions are being tested in trial NCT06944223?

The interventions under investigation include: Kidney stone formers (OTHER), Control cohort (OTHER).

Who is sponsoring clinical trial NCT06944223?

This trial is sponsored by University of Chicago, which has 796 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06944223 being conducted?

This trial has 1 study location across Illinois. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Healthy

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT06944223's enrollment target sits among peer trials

24 791st of 1090 higher than 254 of 1,090 other Healthy trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Healthy trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT02331979 · 24 participants · NA

    Improving Bladder Function in SCI by Neuromodulation

  • NCT03096197 · 24 participants · NA

    Exoskeleton and Spinal Cord Stimulation for SCI

  • NCT03223922 · 24 participants · NA

    Neurocognitive Functioning With Genu-Sparing Whole Brain Radiation Therapy for Brain Metastases

  • NCT03326921 · 24 participants · Phase 1

    HA-1 T TCR T Cell Immunotherapy for the Treatment of Patients With Relapsed or Refractory Acute Leukemia After Donor Stem Cell Transplant

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT06944223, the US trial registry maintained by the National Library of Medicine. NCT06944223 (small enrollment · single site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.