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Study identifier: NCT07580495 Synced from ClinicalTrials.gov · July 28, 2026
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Effect of Collagen Membrane on Ridge Preservation

Condition: Dehiscence · Tooth Extraction · Alveolar Bone Loss  ·  Sponsor: Debora Dias

PhaseNA
Planned participants30
Who can joinAll sexes, 18 Years to 80 Years
Healthy volunteersNo

About this study

This study will evaluate whether adding a resorbable collagen membrane to an anorganic bone-collagen composite (ABCC) graft improves ridge preservation after tooth extraction. Ridge preservation is a procedure used to maintain the shape and volume of the jawbone following tooth removal, which is important for future dental implant placement. Participants will be randomly assigned to receive either ABCC alone or ABCC combined with a collagen membrane. Healing outcomes will be assessed after approximately 4 months using three-dimensional cone beam computed tomography (CBCT) scans. The primary outcome is the change in horizontal ridge dimension (width). Secondary outcomes include vertical and contour changes in ridge dimensions, changes in soft tissue contour assessed with digital scans, postoperative healing and complications (such as wound dehiscence, swelling, or infection), and patient-reported outcomes, including pain and satisfaction. In a subset of participants, bone healing will also be evaluated using laboratory and imaging analyses of bone samples obtained at the time of implant placement. The study will additionally assess whether the treatment allows implant placement in the ideal position without the need for further bone grafting.

This description comes directly from the study's public registry record.

Talk to the study team

Debora R Dias, DDS, PhD  ·  4126488595  ·  deboradias@pitt.edu

Carla Sanchez, MS  ·  4126241179  ·  cab28@pitt.edu

Always discuss trial participation with your own doctor first.

Locations (1)

University of Pittsburgh School of Dental Medicine, Department of Periodontics and Preventive DentistryPittsburgh, Pennsylvania, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT07580495