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    HP:0000787: Nephrolithiasis

    Developed by Shray Alag, The Harker School
    Sections: Correlations, Clinical Trials, and HPO

    Correlations computed by analyzing all clinical trials.

    Navigate: Clinical Trials and HPO


    Correlated Drug Terms (6)


    Name (Synonyms) Correlation
    drug2980 Optifast VLCD Program Wiki 0.71
    drug2355 LithoLyte Wiki 0.71
    drug2990 Oral load of oxalate and sucralose Wiki 0.71
    Name (Synonyms) Correlation
    drug2981 Optifast VLCD Transition Phase Wiki 0.71
    drug547 Baking Soda Wiki 0.71
    drug2399 Low Oxalate Diet Wiki 0.50

    Correlated MeSH Terms (3)


    Name (Synonyms) Correlation
    D053040 Nephrolithiasis NIH 1.00
    D007669 Kidney Calculi NIH 0.82
    D015431 Weight Loss NIH 0.24

    Correlated HPO Terms (1)


    Name (Synonyms) Correlation
    HP:0001824 Weight loss HPO 0.24

    Clinical Trials

    Navigate: Correlations   HPO

    There are 2 clinical trials


    1 Effectiveness of Prescription vs. Non-prescription Urinary Alkalinizing Agents on Kidney Stone Risk

    Randomized treatment trial of baking soda or LithoLyte to determine if baking soda and Litholyte are effective in raising 24 hour urine citrate and pH.

    NCT04095975
    Conditions
    1. Kidney Stone
    Interventions
    1. Dietary Supplement: Baking Soda
    2. Dietary Supplement: LithoLyte
    MeSH:Kidney Calculi Nephrolithiasis
    HPO:Nephrolithiasis

    Primary Outcomes

    Description: Pre-to-post intervention change in 24-hour urine citrate will be measured Reference range of Urine Citrate: 18 years and older: 320-1240 mg/d 1 year and older: greater than or equal to 150 mg/g.

    Measure: Change in 24 hour urine citrate

    Time: Pre and 24 hour post intervention (up to 90 days)

    Description: Pre-to-post intervention change in 24-hour urine pH will be measured Reference range of Urine pH: Age 0 days and up: 5.0-8.0

    Measure: Change in 24 hour urine pH

    Time: Pre and 24 hour post intervention (up to 90 days)

    Secondary Outcomes

    Description: Urine calcium levels will be measured post intervention. Reference range of Urine Calcium: 0-17 years: up to 6.0 mg/kg/24 hours 18 years and up: 100-300 mg/24 hours

    Measure: Post-intervention 24-hour urine calcium

    Time: Enrollment and follow up visit (approximately 90 days)

    Description: Reference range of urine calcium: 0-12 years: 7-31 mg/d Male 13 years and older: 16-49 mg/d Female 13 years and older: 13-40 mg/d

    Measure: 24 hour urine calcium

    Time: Enrollment and follow up visit (approximately 90 days)

    Description: Supersaturation means there are too many salts and not enough fluids in the urine. It's the driving force behind stone formation. Post interventional 24 hour urine supersaturation indices for calcium oxalate will be measured. Reference range: 0-12 years: 7-31 mg/d Male 13 years and older: 16-49 mg/d Female 13 years and older: 13-40 mg/d

    Measure: Post interventional 24 hour urine supersaturation indices for calcium oxalate

    Time: Enrollment and follow up visit (approximately 90 days)

    Description: Supersaturation means there are too many salts and not enough fluids in the urine. It's the driving force behind stone formation. Post interventional 24 hour urine supersaturation indices for calcium phosphatase will be measured. Reference range: Age 18 years and up: 0.4-1.3 g/24 hour

    Measure: Post interventional 24 hour urine supersaturation indices for calcium phosphatase

    Time: Enrollment and follow up visit (approximately 90 days)

    Description: Cost of baking soda versus LithoLyte.

    Measure: Cost of Treatment as measured by USD spent on the interventional drug

    Time: End of study (approximately 90 days)

    Description: Wisconsin Stone-QOL: answers range from a scale of 1-5, or yes/no Study Questionnaire: free text responses, or no/yes/I am no longer taking it

    Measure: Patient acceptability

    Time: End of study (approximately 90 days)
    2 Effect of Weight Loss on Urinary Oxalate Excretion in Obese Calcium Oxalate Kidney Stone

    This protocol seeks to determine if weight reduction with the Optifast VLCD program leads to reduced contribution of endogenous oxalate synthesis to the urinary oxalate pool in obese calcium oxalate stone formers.

    NCT04633811
    Conditions
    1. Kidney Stone
    Interventions
    1. Dietary Supplement: Low Oxalate Diet
    2. Dietary Supplement: Oral load of oxalate and sucralose
    3. Dietary Supplement: Optifast VLCD Program
    4. Dietary Supplement: Optifast VLCD Transition Phase
    MeSH:Kidney Calculi Nephrolithiasis Weight Loss
    HPO:Decreased body weight Nephrolithiasis Weight loss

    Primary Outcomes

    Description: Subjects will ingest a controlled diet low in oxalate and collect 2 x 24-hour urines before and after the Optifast VLCD Program. The utilization of a low oxalate diet allows assessment of the change in contribution of endogenous oxalate synthesis to the urinary oxalate pool.

    Measure: Measurement of 24 hour urinary oxalate excretion

    Time: Day 4

    HPO Nodes


    Reports

    Data processed on December 13, 2020.

    An HTML report was created for each of the unique drugs, MeSH, and HPO terms associated with COVID-19 clinical trials. Each report contains a list of either the drug, the MeSH terms, or the HPO terms. All of the terms in a category are displayed on the left-hand side of the report to enable easy navigation, and the reports contain a list of correlated drugs, MeSH, and HPO terms. Further, all reports contain the details of the clinical trials in which the term is referenced. Every clinical trial report shows the mapped HPO and MeSH terms, which are also hyperlinked. Related HPO terms, with their associated genes, protein mutations, and SNPs are also referenced in the report.

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