Clinical Trials Directory

Trials / Completed

CompletedNCT03897465

Lomatuell Pro® Versus UrgoTul® in the Management of Acute Wounds

Comparative Evaluation of the propertieS of the Contact LAyer Dressing LOMatuell Pro® Versus UrgoTul® in the Management of Acute Wounds

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
183 (actual)
Sponsor
Lohmann & Rauscher · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Comparative evaluation of the propertieS of the contact LAyer dressing LOMatuell Pro® versus UrgoTul® in the management of acute wounds

Detailed description

National, multicenter, prospective, randomized in parallel groups, non-inferiority, open-label investigation study.

Conditions

Interventions

TypeNameDescription
DEVICELomatuell ProPatients will receive Lomatuell Pro dressings during 3 weeks. Lomatuell Pro® may be left in place up to 7 days; additional dressing changes can be performed as often as necessary according to the instruction for use.
DEVICEUrgoTulPatients will receive UrgoTul dressings during 3 weeks. UrgoTul® may be left in place up to 7 days; ; additional dressing changes can be performed as often as necessary according to the instruction for use.

Timeline

Start date
2019-02-11
Primary completion
2020-12-06
Completion
2020-12-06
First posted
2019-04-01
Last updated
2025-10-29
Results posted
2025-02-07

Locations

1 site across 1 country: France

Source: ClinicalTrials.gov record NCT03897465. Inclusion in this directory is not an endorsement.