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Palatal Donor Site Wound Healing Following Periodontal Plastic Surgery Using Amnion-Chorion Membrane

Palate; Wound Clinical Trial

Official title:
Palatal Donor Site Wound Healing Following Periodontal Plastic Surgery Using Amnion-Chorion Membrane: Site- and Patient-Centered Outcomes

Clinical Trial Summary

The purpose of this clinical trial is to assess if donor site healing in the palatal area and patient pain perception are similar or different when using amnio-chorion membrane (ACM) on the donor site after surgery compared to a commonly used commercial hemostatic agent (ActCel Cellulose Gauze).

Clinical Trial Description

Resorbable oxidized cellulose materials are commonly used as hemostatic agents in medicine and dentistry. Surgicel and ActCel are used daily in surgical practice. When these products come in contact with blood, they convert to a gel that expands to cause direct pressure on blood vessels and control bleeding. ActCel is water-soluble and dissolves over a short time period. It can be removed easily when water, saline or hydrogen peroxide is applied.The study team will examine the effects of ACM as a wound dressing for the donor area and compare the rate of epithelialization with and without its use. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05927714
Study type Interventional
Source The University of Texas Health Science Center at San Antonio
Contact Brian Mealey, DDS, MS
Phone 210-450-8736
Email mealey@uthscsa.edu
Status Recruiting
Phase N/A
Start date September 11, 2023
Completion date February 2026
View Details
See also
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