Drug Use-Results Survey on Picoprep® Combination Powder

Overview

The purpose of this survey is to confirm safety and efficacy with patients who are administered the Picoprep® for cleansing of intestinal contents for preparation of colonoscopy and colorectal surgery.

Full Title of Study: “Drug Use-Results Survey on Picoprep® Combination Powder”

Study Type

  • Study Type: Observational
  • Study Design
    • Time Perspective: Prospective
  • Study Primary Completion Date: December 2021

Interventions

  • Drug: Sodium Picosulfate, Magnesium Oxide and Citric Acid
    • Combination powder for oral solution

Arms, Groups and Cohorts

  • Patients administered Picoprep® for bowel cleansing
    • Patients administered Sodium Picosulfate, Magnesium Oxide and Citric Acid for bowel cleansing

Clinical Trial Outcome Measures

Primary Measures

  • Bowel cleansing assessment for colonoscopy
    • Time Frame: 48 hours after drug administration
    • Assessment of each part of large intestine using a bowel cleanliness rating scale
  • Bowel cleansing assessment for colorectal surgery
    • Time Frame: 48 hours after drug administration
    • Assessment of each part of large intestine using a bowel cleanliness rating scale

Participating in This Clinical Trial

Inclusion Criteria

Patients who are administered the Picoprep® for cleansing of intestinal contents for preparation of colonoscopy and colorectal surgery.

Gender Eligibility: All

Minimum Age: N/A

Maximum Age: N/A

Are Healthy Volunteers Accepted: No

Investigator Details

  • Lead Sponsor
    • Ferring Pharmaceuticals
  • Provider of Information About this Clinical Study
    • Sponsor
  • Overall Official(s)
    • Global Clinical Compliance, Study Director, Ferring Pharmaceuticals
  • Overall Contact(s)
    • Global Clinical Compliance, +1 833-548-1402 (US/Canada), DK0-Disclosure@ferring.com

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