Actively Recruiting
Acellular Collagen Matrix as a Tool to Obtain Wound Closure Following Guided Bone Regeneration Procedures
Led by Ohio State University · Updated on 2026-02-13
30
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are evaluating the use of an acellular collagen matrix to improve wound healing after guided bone regeneration (GBR) procedures in patients who need increased bone volume in the jaw before dental implant placement. This study compares healing outcomes between patients whose wound is closed with the acellular matrix versus those who receive traditional surgical closure without it. The study focuses on early wound healing and aims to assess whether the acellular matrix helps prevent shallow vestibulum formation and reduces the need for additional surgeries. During the GBR procedure, bone grafting material is placed in the jawbone defect and covered with a barrier membrane. When the membrane is exposed due to limited tissue coverage, the acellular matrix may be placed over it to aid healing. Patients receive either the acellular matrix covering or standard surgical closure without the matrix, based on their dental surgeon's judgment. Standard postoperative care including antibiotics, pain control, and antiseptic mouthwash is provided. The study collects additional clinical and radiographic measurements before and after surgery, along with patient-reported experience data. Participants will have follow-up visits at 8-10 days, 6-8 weeks, and 4-6 months after surgery, during which wound healing will be assessed through clinical exams, CBCT scans, and implant stability checks. The study will measure healing scores and ridge dimension changes over time. Each visit may last about 40 minutes longer than routine appointments due to research-related assessments. The total observation period lasts up to 4-6 months, ending around the time of implant placement surgery.
CONDITIONS
Brief Title
Acellular Collagen Matrix as a Tool to Obtain Wound Closure Following a Guided Bone Regeneration Procedure
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Have a missing tooth or teeth planned for implant replacement
- Need for guided bone regeneration to increase bone for implant placement
- Systemically healthy with no contraindications for bone grafting or implant surgery
- No chronic sinus problems
- Non-smoker
- No need for removable temporary restorations during wound healing
You will not qualify if you...
- Sufficient bone volume allowing implant placement without GBR
- Need for pre-implant soft tissue grafting to improve soft tissue contours
- Requirement to wear a removable temporary restoration during healing
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Day of surgery
Participants undergo the guided bone regeneration (GBR) procedure where the surgical site is prepared and wound closure is achieved either by using an acellular collagen matrix or conventional surgical closure.
1 visit (in-person)
Duration - 4 to 6 months
Participants are observed for wound healing and clinical outcomes with follow-up visits to evaluate healing score, wound status, ridge dimension changes, and patient experience.
Visits at 8-10 days, 6-8 weeks, and 4-6 months post surgery
Trial Site Locations
Total: 1 location
1
The Ohio State University Graduate Periodontics Clinic
Columbus, Ohio, United States, 43210
Actively Recruiting
Research Team
B
Binnaz Leblebicioglu, DDS, MS, PhD
F
Francesca Racca, DMD
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
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