Drug Use-Results Survey on Picoprep® Combination Powder

NCT ID: NCT03631446

Last Updated: 2022-01-18

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

1298 participants

Study Classification

OBSERVATIONAL

Study Start Date

2017-08-29

Study Completion Date

2021-12-31

Brief Summary

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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.

Detailed Description

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Conditions

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Bowel Cleansing

Study Design

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Observational Model Type

CASE_ONLY

Study Time Perspective

PROSPECTIVE

Study Groups

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Patients administered Picoprep® for bowel cleansing

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

Sodium Picosulfate, Magnesium Oxide and Citric Acid

Intervention Type DRUG

Combination powder for oral solution

Interventions

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Sodium Picosulfate, Magnesium Oxide and Citric Acid

Combination powder for oral solution

Intervention Type DRUG

Other Intervention Names

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Picoprep®

Eligibility Criteria

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Inclusion Criteria

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

ALL

Accepts Healthy Volunteers

No

Sponsors

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Ferring Pharmaceuticals

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Global Clinical Compliance

Role: STUDY_DIRECTOR

Ferring Pharmaceuticals

Locations

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Investigational Site (there may be other sites in this country)

Shibuya City, Tokyo, Japan

Site Status

Countries

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Japan

Other Identifiers

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000311

Identifier Type: -

Identifier Source: org_study_id

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