Status:
UNKNOWN
Pilot Study to Assess Tolerability and Feasibility of Oral Sulfate Solution (SUPREP) in Hospitalized Patients
Lead Sponsor:
University of Virginia
Conditions:
Inpatient Colonoscopy
Oral Sulfate Solution
Eligibility:
All Genders
18-100 years
Phase:
NA
Brief Summary
This study will test the efficacy, tolerability, and feasibility of an oral sulfate solution (SUPREP) for inpatient colonoscopy preparation, compared to the standard of care (GoLytely). The hypothesis...
Eligibility Criteria
Inclusion
- Patients will be approached with consent for the study only if there is a clinical indication for pursuing an inpatient colonoscopy
Exclusion
- Inability to consent (patient or POA)
Key Trial Info
Start Date :
August 1 2020
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
July 30 2021
Estimated Enrollment :
124 Patients enrolled
Trial Details
Trial ID
NCT04504292
Start Date
August 1 2020
End Date
July 30 2021
Last Update
August 11 2020
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