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Completed

NCT Number: NCT05081960

Evaluating the Vitamin K2 Status of Calcium-based Stone Formers

This is an observation, single site-study with one study visit during which all data and samples will be collected. Study participants will be asked to provide blood, urine, and fecal samples so that the investigators may study the differences in the gut microbiota, vitamin K2 levels, and other parameters between participants who form kidney stones and those who do not.

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Key information

About this study

It is hypothesized that calcium-based stone formers will have an altered fecal gut microbiota compared to non-stone former controls. This altered microbiota will have a lower abundance of bacteria that produce menaquinones (vitamin K2), thus stone formers will also have a different blood menaquinone profile compared to controls. Ultimately, the different levels of menaquinones will result in increased inactive Matrix Gla protein (dp-ucMGP), which is a key protein that sequesters free calcium. To test this hypothesis, calcium-based stone former and non-stone forming controls will be recruited to a single site, observation study to collect urine, blood, and fecal samples. These samples will be used to determine dp-ucMGP levels, menaquinone profiles, the composition of the gut microbiota, and other parameters of interest.

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Male/Female, 18 - 65 years old
  • No self-reported kidney stones during their lifetime (controls)
  • Ultrasound examination confirming absence of kidney stones (controls)
  • Have had at least 1 incidence of a clinically confirmed calcium-based kidney stone in the last 12 months (stone formers)
  • Ability to collect a clean catch urine sample
  • Prescription and over-the-counter drugs unchanged for ≥30 days
  • Willingness to provide medical information, blood, urine, and fecal samples

Exclusion criteria

  • Current, or within 30 days, use of antibiotics or antifungals
  • Current, or within 30 days, use of vitamin K antagonists
  • Current probiotic use or any use within 14 days of screening sample collection should be recorded
  • A history or currently undergoing immunosuppressive drug therapy, chemotherapy, or radiation therapy 2021-06-29 1.0 Page 4 of 6
  • Fecal incontinence
  • History of disorder with abnormal calcium regulation such as hyperparathyroidism, active malignancy, or osteoporosis.

Treatment and study plan

Primary outcomes

  1. Fecal microbiota composition of stone-formers and controls

    Time frame: At baseline only

    Fecal samples will be collected using out validated toilet paper method. Microbial DNA will be extracted and sequenced using next-generation sequencing.

  2. Concentration of urine dp-ucMGP (dephosphorylated-uncarboxylated Matrix Gla Protein)

    Time frame: At baseline only

    dp-ucMGP will be quantified using an enzyme-linked immunosorbent assay

  3. Concentration of blood dp-ucMGP (dephosphorylated-uncarboxylated Matrix Gla Protein)

    Time frame: At baseline only

    dp-ucMGP will be quantified using an enzyme-linked immunosorbent assay

  4. Concentration of blood total osteocalcin (OC)

    Time frame: At baseline only

    Total OC will be quantified using an enzyme-linked immunosorbent assay

  5. Concentration of blood undercarboxylated osteocalcin (ucOC)

    Time frame: At baseline only

    ucOC will be quantified using an enzyme-linked immunosorbent assay

  6. Concentration of urine total osteocalcin (OC)

    Time frame: At baseline only

    Total OC will be quantified using an enzyme-linked immunosorbent assay

  7. Concentration of urine undercarboxylated osteocalcin (ucOC)

    Time frame: At baseline only

    ucOC will be quantified using an enzyme-linked immunosorbent assay

  8. Concentration of blood menaquinones (vitamin K2) - MK-4

    Time frame: At baseline only

    Menaquinones will be quantified using liquid chromatography with mass spectrometry or fluorescence.

  9. Concentration of blood menaquinones (vitamin K2) - MK-7

    Time frame: At baseline only

    Menaquinones will be quantified using liquid chromatography with mass spectrometry or fluorescence.

  10. Concentration of blood menaquinones (vitamin K2) - MK-8

    Time frame: At baseline only

    Menaquinones will be quantified using liquid chromatography with mass spectrometry or fluorescence.

  11. Concentration of blood menaquinones (vitamin K2) - MK-9

    Time frame: At baseline only

    Menaquinones will be quantified using liquid chromatography with mass spectrometry or fluorescence.

  12. Concentration of blood menaquinones (vitamin K2) - MK-10

    Time frame: At baseline only

    Menaquinones will be quantified using liquid chromatography with mass spectrometry or fluorescence.

  13. Concentration of blood menaquinones (vitamin K2) - MK-11

    Time frame: At baseline only

    Menaquinones will be quantified using liquid chromatography with mass spectrometry or fluorescence.

  14. Concentration of blood menaquinones (vitamin K2) - MK-12

    Time frame: At baseline only

    Menaquinones will be quantified using liquid chromatography with mass spectrometry or fluorescence.

  15. Concentration of blood menaquinones (vitamin K2) - MK-13

    Time frame: At baseline only

    Menaquinones will be quantified using liquid chromatography with mass spectrometry or fluorescence.

Secondary outcomes

  1. Concentration of blood fetuin A

    Time frame: At baseline only

    Fetuin A will be quantified using enzyme-linked immunosorbent assay

  2. Concentration of urine fetuin A

    Time frame: At baseline only

    Fetuin A will be quantified using enzyme-linked immunosorbent assay

  3. Percentage of blood Hemoglobin A1C (HbA1c)

    Time frame: At baseline only

    HbA1c will be quantified in the core laboratory as per established protocols

  4. Total plasma calcium

    Time frame: At baseline only

    Calcium levels will be quantified in the core laboratory

  5. Concentration of ionized calcium in blood

    Time frame: At baseline only

    Calcium levels will be quantified in the core laboratory

  6. Concentration of blood albumin

    Time frame: At baseline only

    Albumin levels will be quantified in the core laboratory as per established protocols

  7. Concentration of urinary γ-carboxyglutamic acid

    Time frame: At baseline only

    γ-carboxyglutamic acid will be quantified using high-performance liquid chromatography and normalized to creatinine

  8. Concentration of urinary creatinine

    Time frame: At baseline only

    Creatinine will be quantified using high-performance liquid chromatography

  9. Concentration of urinary oxalate

    Time frame: At baseline only

    Oxalate will be quantified using high-performance liquid chromatography and normalized to creatinine

  10. Concentration of urinary phosphate

    Time frame: At baseline only

    Phosphate will be quantified in the core laboratory as per established protocols

Sponsors and collaborators

Lead sponsor

London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's

Other

Collaborators

  • St. Joseph's Health Care London

Registry information

Important dates

Study start
2022
Primary completion
2023
Study completion
2025
First posted
Oct 18, 2021
Registry last updated
Jul 22, 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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