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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Pilot Study to Assess Tolerability and Feasibility of Oral Sulfate Solution (SUPREP) in Hospitalized Patients | DecenTrialz