Trials / Unknown
UnknownNCT03742726
Study Assessing the Safety and Performance of Smart Matrix®
Study Assessing the Safety and Performance of Smart Matrix® Dermal Replacement Scaffold in the Treatment of Full-Thickness Wounds Arising From Surgical Excision of Basal Cell or Squamous Cell Carcinomas in Male and Female Adult Patients
- Status
- Unknown
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 32 (actual)
- Sponsor
- Smart Matrix Limited · Academic / Other
- Sex
- All
- Age
- 18 Years – 90 Years
- Healthy volunteers
- Not accepted
Summary
Smart Matrix is a sterile, single layer dermal replacement scaffold. The scaffold consists of a porous matrix of cross-linked human fibrin plus alginate that has been designed and optimised to facilitate wound closure and healing through cellular invasion.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Smart Matrix scaffold | Smart Matrix dermal replacement scaffold |
Timeline
- Start date
- 2018-10-12
- Primary completion
- 2021-07-01
- Completion
- 2022-01-01
- First posted
- 2018-11-15
- Last updated
- 2021-02-21
Locations
4 sites across 1 country: United Kingdom
Source: ClinicalTrials.gov record NCT03742726. Inclusion in this directory is not an endorsement.