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Amnion-Chorion Membrane for Palate Wound Healing
N/A
Recruiting
Led By Brian Mealey, DDS, MS
Research Sponsored by The University of Texas Health Science Center at San Antonio
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 24, 48 and 72 hours post-surgery
Summary
This trial is testing if a special tissue bandage helps mouth surgery wounds heal better and reduces pain compared to a common gauze. The study focuses on patients who need healing in the roof of their mouth after surgery. The special tissue bandage has been used in various oral surgeries for tissue regeneration.
Who is the study for?
This trial is for adults aged 18-89 needing gum surgery in the mouth area from back molar to back molar, whether they have teeth, implants, or none. Participants can be non-smokers or light smokers (less than 10 cigarettes a day), including women who are not pregnant and either post-menopausal, had tubal ligation/hysterectomy, or use contraception. They must also be able to follow up and own a smartphone.
What is being tested?
The study compares two methods of healing after gum surgery: using an amnion-chorion membrane (ACM) versus ActCel Cellulose Gauze—a common bleeding control product. It aims to see if there's a difference in how the palate heals and how much pain patients feel with each treatment.
What are the potential side effects?
While specific side effects aren't listed here, typical risks may include discomfort at the wound site, potential infection risk due to open wounds in the mouth area, allergic reactions to materials used like ACM or gauze, and general complications related to oral surgeries.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 24, 48 and 72 hours post-surgery
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~24, 48 and 72 hours post-surgery
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Post-operative pain
Wound healing time
Trial Design
2Treatment groups
Active Control
Placebo Group
Group I: Use Amnio Chorion Membrane (ACM) with hemostatic agentActive Control2 Interventions
ACM or amnion-only membranes have been used in oral surgical procedures primarily because they contain a host of growth factors that play a role in normal wound healing.
Group II: Use of ActCel Cellulose Gauze (Commercial Hemostatic Agent)Placebo Group1 Intervention
Palatal wound dressing with hemostatic agent
Research Highlights
Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
The most common treatments for palate wounds, such as the Amnio-Chorion Membrane (ACM), work by promoting healing and reducing inflammation. ACM contains growth factors and anti-inflammatory cytokines that accelerate tissue regeneration and minimize inflammatory responses.
This is crucial for palate wound patients as it leads to faster recovery, reduced pain, and lower risk of infection. Other treatments, like hemostatic agents, primarily focus on controlling bleeding and providing a scaffold for new tissue growth, further aiding in the healing process.
The effects of lyophilized homograft amniotic membrane on wound healing on rabbits.
The effects of lyophilized homograft amniotic membrane on wound healing on rabbits.
Find a Location
Who is running the clinical trial?
The University of Texas Health Science Center at San AntonioLead Sponsor
475 Previous Clinical Trials
92,242 Total Patients Enrolled
Brian Mealey, DDS, MSPrincipal InvestigatorUniversity of Texas Health Science Center San Antonio
1 Previous Clinical Trials
120 Total Patients Enrolled
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- I am a nonsmoker, former smoker, or smoke less than 10 cigarettes a day.I need a dental procedure in my upper or lower jaw, from back to front, regardless of having teeth or implants.I am a woman who cannot become pregnant due to surgery or menopause.I smoke more than 10 cigarettes a day.I am between 18 and 89 years old.
Research Study Groups:
This trial has the following groups:- Group 1: Use Amnio Chorion Membrane (ACM) with hemostatic agent
- Group 2: Use of ActCel Cellulose Gauze (Commercial Hemostatic Agent)
Awards:
This trial has 0 awards, including:Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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