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Clinical Trial Summary

In this study the investigators propose to use a daily dose of 45 mg (30 mg at 8 AM and 15 mg at 4 PM). This relatively small well-tolerated dose is likely to persistently increase urine volume and reduce urine supersaturation and to be well tolerated by patients with kidney stone disease and normal renal function (see below). The twice-daily (8 AM and 4 PM) regimen is designed to produce a maximal AVP inhibition on waking with a gradual fall-off of effect during the night. To this end, a higher dose is used in the morning, with a lower dose in the afternoon.


Clinical Trial Description

n/a


Study Design

Allocation: Randomized, Intervention Model: Crossover Assignment, Masking: Double Blind (Subject, Caregiver, Investigator), Primary Purpose: Basic Science


Related Conditions & MeSH terms


NCT number NCT02096965
Study type Interventional
Source Mayo Clinic
Contact
Status Completed
Phase Phase 1
Start date March 2014
Completion date November 2015

See also
  Status Clinical Trial Phase
Completed NCT00381849 - Use of an Herbal Preparation to Prevent and Dissolve Kidney Stones Phase 1/Phase 2
Recruiting NCT06331546 - Gut Oxalate Absorption in Calcium Oxalate Stone Disease N/A
Recruiting NCT06330246 - O. Formigenes Colonization in Calcium Oxalate Kidney Stone Disease N/A