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Multicenter Pilot Study to Describe the Performance of a New Device in Patients With Colostomy

NCT02602236 · Status: TERMINATED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 31

Last updated 2017-02-06

No results posted yet for this study

Summary

The study evaluates the efficacy of a new 2-piece appliance in patients with colostomy.

Conditions

  • Colostomy

Interventions

DEVICE

AOS-C2000-B

1 base plate for 2 or 3 days and 1 to 4 collection special pouch per day

Sponsors & Collaborators

  • BBraun Medical SAS

    lead INDUSTRY

Principal Investigators

  • Mahaut LECONTE, MD · University Hospital of Paris - Cochin

Study Design

Allocation
NA
Purpose
SUPPORTIVE_CARE
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-11-30
Primary Completion
2016-10-31
Completion
2016-10-31

Countries

  • France

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02602236 on ClinicalTrials.gov