St. Joseph's Health Care London
London, Ontario, N6J 3T9, Canada
NCT Number: NCT05081960
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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Notify Me18 year–65 year
All sexes
Observational
London, Ontario, N6J 3T9, Canada
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.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
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.
Time frame: At baseline only
dp-ucMGP will be quantified using an enzyme-linked immunosorbent assay
Time frame: At baseline only
dp-ucMGP will be quantified using an enzyme-linked immunosorbent assay
Time frame: At baseline only
Total OC will be quantified using an enzyme-linked immunosorbent assay
Time frame: At baseline only
ucOC will be quantified using an enzyme-linked immunosorbent assay
Time frame: At baseline only
Total OC will be quantified using an enzyme-linked immunosorbent assay
Time frame: At baseline only
ucOC will be quantified using an enzyme-linked immunosorbent assay
Time frame: At baseline only
Menaquinones will be quantified using liquid chromatography with mass spectrometry or fluorescence.
Time frame: At baseline only
Menaquinones will be quantified using liquid chromatography with mass spectrometry or fluorescence.
Time frame: At baseline only
Menaquinones will be quantified using liquid chromatography with mass spectrometry or fluorescence.
Time frame: At baseline only
Menaquinones will be quantified using liquid chromatography with mass spectrometry or fluorescence.
Time frame: At baseline only
Menaquinones will be quantified using liquid chromatography with mass spectrometry or fluorescence.
Time frame: At baseline only
Menaquinones will be quantified using liquid chromatography with mass spectrometry or fluorescence.
Time frame: At baseline only
Menaquinones will be quantified using liquid chromatography with mass spectrometry or fluorescence.
Time frame: At baseline only
Menaquinones will be quantified using liquid chromatography with mass spectrometry or fluorescence.
Time frame: At baseline only
Fetuin A will be quantified using enzyme-linked immunosorbent assay
Time frame: At baseline only
Fetuin A will be quantified using enzyme-linked immunosorbent assay
Time frame: At baseline only
HbA1c will be quantified in the core laboratory as per established protocols
Time frame: At baseline only
Calcium levels will be quantified in the core laboratory
Time frame: At baseline only
Calcium levels will be quantified in the core laboratory
Time frame: At baseline only
Albumin levels will be quantified in the core laboratory as per established protocols
Time frame: At baseline only
γ-carboxyglutamic acid will be quantified using high-performance liquid chromatography and normalized to creatinine
Time frame: At baseline only
Creatinine will be quantified using high-performance liquid chromatography
Time frame: At baseline only
Oxalate will be quantified using high-performance liquid chromatography and normalized to creatinine
Time frame: At baseline only
Phosphate will be quantified in the core laboratory as per established protocols
London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's
Other
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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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