The following info and data is provided "as is" to help patients around the globe.
We do not endorse or review these studies in any way.
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
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).
Minimum Age: 18 Years
Eligible Ages: ADULT, OLDER_ADULT
Sex: ALL
Healthy Volunteers: No
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
Name: Annamaria Kausz, MD, MS
Affiliation: Allena Pharmaceuticals
Role: STUDY_DIRECTOR