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The Affect of Low-Volume Bowel Preparation for Hospitalized Patients Colonoscopies

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Mayo Clinic

Status

Terminated

Conditions

Colonoscopy

Treatments

Drug: Low volume prep (Prepopik)
Drug: High volume prep (Golytely)
Drug: Moderate volume prep (Moviprep)

Study type

Interventional

Funder types

Other

Identifiers

NCT01978509
13-003983

Details and patient eligibility

About

The purpose of this study is to compare the efficacy of a low-volume bowel preparation versus a high-volume bowel preparation for bowel cleansing on hospitalized patients undergoing colonoscopies.

Enrollment

32 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  1. Inpatient colonoscopy
  2. Age 18 years and older
  3. Able to give consent
  4. Split dose colonoscopies for all patients

Exclusion criteria

  1. Unable to give consent
  2. Pregnant or lactating women
  3. Renal impairment (GFR <30)
  4. Ileus
  5. Ascites
  6. Toxic megacolon
  7. Gastrointestinal obstruction
  8. Allergy to study drugs
  9. Toxic colitis
  10. Not able to split the dose of bowel preparations to be used
  11. Contraindication to bowel preparation
  12. Risk for aspiration
  13. Risk of severe cardiac arrhythmias

Trial design

Primary purpose

Diagnostic

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

32 participants in 3 patient groups

Low volume prep (Prepopik)
Active Comparator group
Description:
Low volume prep for colonoscopy (Prepopik)
Treatment:
Drug: Low volume prep (Prepopik)
Moderate volume prep (Moviprep)
Active Comparator group
Description:
Moderate volume prep for colonoscopy (Moviprep)
Treatment:
Drug: Moderate volume prep (Moviprep)
High volume prep (Golytely)
Active Comparator group
Description:
High volume prep for colonoscopy (Golytely)
Treatment:
Drug: High volume prep (Golytely)

Trial documents
1

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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