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Evaluating the Barrier Function, Regenerative Capacity, and Soft Tissue Outcomes of Acellular Dermal Matrix

University of Alabama at Birmingham · NCT07613047

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Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.

Key facts

Compensation
Not posted. Ask the study team before screening.
Who can join
Ages 18–85 · All sexes
Healthy volunteers
Accepted
Study type
Interventional · Not applicable
Target enrollment
70
US sites recruiting
1
Study start
September 10, 2026
Record last updated
October 23, 2026

Status re-checked against ClinicalTrials.gov within the last 12 hours.

What the study is about

This investigator-initiated study will compare ADM and resorbable cross-linked collagen membrane barriers for guided bone regeneration at atrophic lateral ridge augmentation sites.

Being studied: Guided Bone Regeneration with ADM (AlloDerm) as a barrier; Guided Bone Regeneration with Resorbable Crosslinked Collagen Matrix (Mem-Lok) as a barrier

Conditions: Acellular Dermal Matrix; Bone Grafting; Soft Tissue Grafting

Eligibility criteria

Copied from the official record. The study team makes the final decision at screening.

Show full criteria

Inclusion Criteria

  • English speaking
  • At least 18 years old
  • Must be a patient of the UAB Dental School
  • Able to read and understand informed consent document
  • Patients presenting with a diagnosed need horizontal ridge augmentation with GBR without simultaneous implant placement, to allow for future dental implant placement.
  • Presence of periodontally healthy, non-carious neighboring teeth and/or healthy restored dental implants on either side of the edentulous span planned for GBR, or unhealthy adjacent teeth to be extracted during the same visit.
  • ≤4 mm ridge width in a Seibert Class I Edentulous span19
  • No anticipated need for surgical and/or endodontic care at planned teeth adjacent to the proposed surgical site during the study period.

Exclusion Criteria

  • Non-English speaking
  • Less than 18 years old
  • Smokers/nicotine users (defined as currently reporting use of any form of tobacco/nicotine products)
  • Patients with systemic pathologies or conditions contraindicating oral surgical procedures or adversely affecting wound healing, including:
  • Uncontrolled diabetes (HbA1c > 7%)
  • Untreated periodontal disease
  • History of head/neck radiation
  • IV bisphosphonates
  • Immunocompromised state
  • Pregnancy
  • Acute infection at site
  • Documented or suspected allergy or sensitivity to any study product

Recruiting US locations

  • University of Alabama at Birmingham

    Birmingham, AL 35294

    Site contact: Maria Geisinger, DDS, MS · 205-934-4984 · miagdds@uab.edu

Study contacts (from the official record)

  • Maria Geisinger, DDS, MS · 205-934-4984 · miagdds@uab.edu
  • Sarah Startley, DMD · 205-975-8711 · ss1971@uab.edu
Evaluating the Barrier Function, Regenerative Capacity, and Soft… (NCT07613047) | Bored Studies