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Spots Global Cancer Trial Database for A Pilot Study of Oxalate Absorption in Secondary Hyperoxaluria

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Trial Identification

Brief Title: A Pilot Study of Oxalate Absorption in Secondary Hyperoxaluria

Official Title: A Pilot Study of Oxalate Absorption in Secondary Hyperoxaluria

Study ID: NCT03095885

Interventions

Test Meal

Study Description

Brief Summary: Identify individuals with greater absorption of oxalate based on increase in urinary oxalate excretion in response to a controlled oxalate-rich test meal.

Detailed Description: This was a prospective 4-day study of oxalate absorption in subjects with secondary hyperoxaluria. Subjects visited the research center three times for outpatient visits (Screening, Test Day 3, Day 4). Subjects were instructed to follow a low-oxalate diet, consuming only study-specified food choices that had low or no oxalate and controlled calcium content Days 1 through 4 (Baseline Period through the Day 4 clinic visit) and, on Test Day 3, consumed an oxalate-rich test meal. Subjects performed three 24-hour urine collections during Screening, Baseline Day 2, and Test Day 3. Test Day 3 included the oxalate-rich test meal and the subject collected a 24-hour urine separated into 4 urine collection intervals. (Pre-test meal, post-test meal to 4 hours, 4-6 hours post test meal and remaining time to complete 24 hours).

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Urological Associates of Southern Arizona, PC, Tucson, Arizona, United States

Applied Research Center of Arkansas, Inc., Little Rock, Arkansas, United States

Regional Urology, LLC, Shreveport, Louisiana, United States

Omega Medical Research, Warwick, Rhode Island, United States

Urology of Virginia, Virginia Beach, Virginia, United States

Contact Details

Name: Annamaria Kausz, MD, MS

Affiliation: Allena Pharmaceuticals

Role: STUDY_DIRECTOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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