NCT00766727

Clinical Evaluation of the GLYDe Dressing for Post-surgical Incision Care

• Status: Completed
• Phase: N/A
• Study type: Interventional
• Enrollment: 12 (actual)
• Sponsor: Neodyne Biosciences, Inc. · Industry
• Sex: All
• Age: 18 Years – 65 Years
• Healthy volunteers: Not accepted

Summary

This study will evaluate a new dressing to be used for post-incision care for abdominoplasty patients. The hypothesis is that this dressing will minimize scar formation.

Detailed description

This study will evaluate a new dressing in up to 30 patients who have undergone an abdominoplasty procedure. They will wear the dressing through 8 weeks post surgery and the scar will be evaluated at 3 months post surgery.

Conditions

• Post Surgical Incisions From Abdominoplasty Procedures

Interventions

Type	Name	Description
DEVICE	GLYDe Dressing	Wound dressing intended to minimize scar formation

Timeline

• Start date: 2008-10-01
• Primary completion: 2009-11-01
• Completion: 2010-03-01
• First posted: 2008-10-06
• Last updated: 2020-12-14
• Results posted: 2020-12-14

Locations

1 site across 1 country: United States

Regulatory

• FDA-regulated device study