Comparison Study of 3 Ostomy Products

NCT01691729 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 26

Last updated 2022-12-07

No results posted yet for this study

Summary

To purpose of the study is to evaluate and compare the efficacy of three ostomy accessory products.

Conditions

  • Ostomy

Interventions

DEVICE

Ostomy accessory

Wearing each of the devices for 10 days each

Sponsors & Collaborators

  • ConvaTec Inc.

    lead INDUSTRY

Principal Investigators

  • Kim Peters · ConvaTec Inc.

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2012-09-30
Primary Completion
2012-11-30
Completion
2012-11-30

Countries

  • United States

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 NCT01691729 on ClinicalTrials.gov