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Single Blind, Randomized, Controlled Trial of Conventional Versus Split-Dose Bowel Preparation for Inpatient Colonoscopy


Phase 4
18 Years
N/A
Open (Enrolling)
Both
Gastrointestinal Hemorrhage, Colon Cancer, Diverticulosis

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Trial Information

Single Blind, Randomized, Controlled Trial of Conventional Versus Split-Dose Bowel Preparation for Inpatient Colonoscopy


Inclusion Criteria:



- any diagnosis for which colonoscopy is indicated

Exclusion Criteria:

- ileus

- severe colitis/toxic megacolon

- gastric retention

- bowel perforation

- gastrointestinal obstruction

- gastroparesis that precludes oral bowel preparation

- pregnant or lactating women

- allergy to polyethylene glycol.

- unable to give consent

Type of Study:

Interventional

Study Design:

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Caregiver), Primary Purpose: Diagnostic

Outcome Measure:

Quality of colon cleansing

Outcome Time Frame:

24 hours from study enrollment

Safety Issue:

No

Authority:

United States: Institutional Review Board

Study ID:

10-041

NCT ID:

NCT01169220

Start Date:

July 2010

Completion Date:

July 2012

Related Keywords:

  • Gastrointestinal Hemorrhage
  • Colon Cancer
  • Diverticulosis
  • Colonoscopy
  • Bowel preparation
  • Colonic Neoplasms
  • Diverticulum
  • Gastrointestinal Hemorrhage
  • Hemorrhage

Name

Location

Santa Clara Valley Medical CenterSan Jose, California  95128