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

> **NCT04504292** · NA · UNKNOWN · sponsor: **University of Virginia** · enrollment: 124 (estimated)

## Conditions studied

- Inpatient Colonoscopy
- Oral Sulfate Solution
- Polyethelene Glycol

## Interventions

- **DRUG:** SUPREP Bowel Prep Kit
- **DRUG:** Golytely Oral Product

## Key facts

- **NCT ID:** NCT04504292
- **Lead sponsor:** University of Virginia
- **Sponsor class:** OTHER
- **Phase:** NA
- **Study type:** INTERVENTIONAL
- **Status:** UNKNOWN
- **Start date:** 2020-08-01
- **Primary completion:** 2021-05-30
- **Final completion:** 2021-07-30
- **Target enrollment:** 124 (ESTIMATED)
- **Last updated:** 2020-08-11


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT04504292

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT04504292, "Pilot Study to Assess Tolerability and Feasibility of Oral Sulfate Solution (SUPREP) in Hospitalized Patients". Retrieved via AI Analytics 2026-05-26 from https://api.ai-analytics.org/clinical/NCT04504292. Licensed CC0.

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