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
| Type | Name | Description |
|---|---|---|
| DEVICE | Lomatuell Pro | Patients 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. |
| DEVICE | UrgoTul | Patients 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.