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Procedure

Allograft Material for Gum Recession

N/A
Waitlist Available
Led By Angela Palaiologou-Gallis, 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 baseline to 12 months
Awards & highlights

Study Summary

This trial tests two routine care procedures for treating gingival recession in patients who need root coverage.

Who is the study for?
This trial is for adults aged 18-89 with gum recession who need root coverage. It's open to nonsmokers, former smokers, and those smoking less than 10 cigarettes a day. Women must be non-pregnant, post-menopause, or have had certain procedures to prevent pregnancy.Check my eligibility
What is being tested?
The study compares two standard care allograft materials (ADM-D and ADM-S) used in dental surgery for treating gum recession. Patients will randomly receive one of these treatments on different sides of the same dental arch.See study design
What are the potential side effects?
As the interventions involve routine dental procedures using allograft materials, potential side effects may include swelling, discomfort at the site of surgery, infection risk, and possible allergic reactions.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~baseline to 12 months
This trial's timeline: 3 weeks for screening, Varies for treatment, and baseline to 12 months for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Keratinized tissue width
Percentage root coverage

Trial Design

2Treatment groups
Active Control
Placebo Group
Group I: Test Group:Acellular Dermal Matrix - Deep cut (ADM-D)Active Control1 Intervention
The use of a deep cut ADM for root coverage gingival plastic procedures.
Group II: Control Group: Acellular Dermal Matrix - Superficial cut (ADM-S)Placebo Group1 Intervention
A commonly used allograft material is the Acellular Dermal Matrix (ADM) which is harvested from human donor dermal tissues. Most commercially available ADM products are superficial cuts.

Find a Location

Who is running the clinical trial?

The University of Texas Health Science Center at San AntonioLead Sponsor
452 Previous Clinical Trials
91,404 Total Patients Enrolled
Angela Palaiologou-Gallis, DDS, MSPrincipal InvestigatorUniversity of Texas Health Science Center San Antonio
1 Previous Clinical Trials
26 Total Patients Enrolled

Media Library

Superficial and Deep Cut Acellular Dermal Matrices (Procedure) Clinical Trial Eligibility Overview. Trial Name: NCT05956496 — N/A
Gum Recession Research Study Groups: Test Group:Acellular Dermal Matrix - Deep cut (ADM-D), Control Group: Acellular Dermal Matrix - Superficial cut (ADM-S)
Gum Recession Clinical Trial 2023: Superficial and Deep Cut Acellular Dermal Matrices Highlights & Side Effects. Trial Name: NCT05956496 — N/A
Superficial and Deep Cut Acellular Dermal Matrices (Procedure) 2023 Treatment Timeline for Medical Study. Trial Name: NCT05956496 — N/A

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.

Is there a possibility of enrolling in this experiment presently?

"Data on clinicaltrials.gov verifies that this trial ceased recruitment on July 13th, 2023 after initially being posted August 1st of the same year. Although no longer taking partcipants, 42 other studies are presently looking for patients to take part in their trials."

Answered by AI

Does the age criterion for this medical experiment preclude those over 79?

"According to the conditions for inclusion in this trial, prospective patients should be older than 18 and younger than 89."

Answered by AI

What characteristics make an individual a viable participant in this clinical trial?

"Aspirants to this clinical trial should have gingival recession and must be between 18-89 years old. The recruitment of participants is expected to reach 20 people in total."

Answered by AI

Who else is applying?

What site did they apply to?
University of Texas Health Science Center at San Antonio
What portion of applicants met pre-screening criteria?
Met criteria
Recent research and studies
clinicaltrials.govStudy
Gingival Augmentation and Root Coverage With Superficial and Deep Cut Acellular Dermal Matrices
Angela Palaiologou-Gallis, DDS, MS 2023. "Gingival Augmentation and Root Coverage With Superficial and Deep Cut Acellular Dermal Matrices". ClinicalTrials.gov. https://clinicaltrials.gov/ct2/show/NCT05956496.
~4 spots leftby Apr 2025
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