Trials / Terminated
TerminatedNCT04890769
Clinical Study of Moisture Sensor Dressing Used for Exuding Wounds
Post Market Clinical Follow-up (PMCF) Study for DryMax Sensor
- Status
- Terminated
- Phase
- —
- Study type
- Observational
- Enrollment
- 4 (actual)
- Sponsor
- Fredrik Iredahl · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
Observational prospective study of the clinical use of a wound dressing with a moisture sensor for use on exuding wounds.
Detailed description
The PMCF study will be performed as a prospective and open study of a wound dressing with a moisture sensor on exuding wounds. Using DryMax Sensor and the display indication - advisory only - might influence the clinician's workflow and the patient's engagement in their care. The PMCF study aims to study the use of the sensor in the clinical procedure of dressing changes in one or more healthcare settings. To study how the new product is received, and how it is used in the workflow, related to its clinical performance. Furthermore, the aim is to gather safety-related clinical data for common harms within exudate management.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Moisture sensor wound dressing | Clinical procedure for change of wound dressing |
Timeline
- Start date
- 2021-05-21
- Primary completion
- 2022-02-22
- Completion
- 2022-02-22
- First posted
- 2021-05-18
- Last updated
- 2022-03-18
Locations
1 site across 1 country: Sweden
Source: ClinicalTrials.gov record NCT04890769. Inclusion in this directory is not an endorsement.