Clinical Trials Directory

Trials / Completed

CompletedNCT01841567

Post Market Clinical Follow-up Study

A Multi-centre, Post CE-mark, Open Investigation to Evaluate the Performance of a Flexible Self-adherent Absorbent Dressing Coated With a Soft Silicone Layer After Hip or Knee Arthroplasty

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
60 (actual)
Sponsor
Molnlycke Health Care AB · Industry
Sex
All
Age
45 Years
Healthy volunteers
Not accepted

Summary

The overall rationale for this study is to evaluate the clinical performance potential for Mepilex Border Post-Op in the ability to minimise the risk of blistering, maceration and less dressing change due to high absorption capacity. This study is a part of Post Market Clinical Follow-Up (PMCF).

Conditions

Interventions

TypeNameDescription
DEVICEMepilex border post. op
DEVICEMepilex border post op

Timeline

Start date
2013-04-01
Primary completion
2013-09-01
Completion
2013-09-01
First posted
2013-04-26
Last updated
2014-09-30
Results posted
2014-09-30

Locations

1 site across 1 country: Germany

Source: ClinicalTrials.gov record NCT01841567. Inclusion in this directory is not an endorsement.

Post Market Clinical Follow-up Study (NCT01841567) · Clinical Trials Directory