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Trials / Active Not Recruiting

Active Not RecruitingNCT06600152

Safety of Microporous Annealed Particle (MAP) Wound Matrix in Patients With Clean Surgical Wounds.

A Randomized, Open-label, Investigational Safety Evaluation of the Microporous Annealed Particle (MAP) Wound Matrix (TT101) Device as a Volumetric Biomaterial Scaffold Applied to Clean Wounds After Skin Cancer Surgery With Mohs Micrographic Surgery (MMS) Compared to Control.

Status
Active Not Recruiting
Phase
N/A
Study type
Interventional
Enrollment
40 (actual)
Sponsor
Tempo Therapeutics · Industry
Sex
All
Age
22 Years
Healthy volunteers
Not accepted

Summary

A randomized, open-label, investigational safety evaluation of the Microporous Annealed Particle (MAP) Wound Matrix (TT101) device as a volumetric biomaterial scaffold applied to clean wounds after skin cancer surgery with Mohs micrographic surgery (MMS) compared to control.

Conditions

Interventions

TypeNameDescription
DEVICEMAP Wound MatrixThe MAP Wound Matrix is indicated for the management of full thickness wounds, including surgical sites, donor skin graft sites, wound dehiscence, lacerations, and draining wounds. The application of MAP Wound Matrix will occur immediately after Mohs surgery once hemostasis has been achieved
DEVICEDuoDermDuoDerm is a hydrocolloid dressing will be topically applied to the wound immediately following Mohs surgery according to the manufacturer\'s instructions.

Timeline

Start date
2024-08-26
Primary completion
2026-08-30
Completion
2026-08-30
First posted
2024-09-19
Last updated
2025-08-11

Locations

3 sites across 1 country: United States

Regulatory

Source: ClinicalTrials.gov record NCT06600152. Inclusion in this directory is not an endorsement.