Clinical Trials Logo

Clinical Trial Summary

The purpose of this study is to prospectively evaluate whether including an allogeneic gum graft (PerioDerm*) during dental implant therapy improves implant health and appearance. On the day of implant surgery, participating subjects will be randomized to either receive or not receive a supplemental gum graft along with the implant. Participating subjects will also be asked to complete a brief (about 15 questions) oral health questionnaire. Participating subjects will return to the clinic about 8 weeks post surgery for digital crown impressions and again at 11-13 weeks after surgery for crown placement. Participating subjects will also return to clinic at 1 year after implant placement for implant evaluation. At this final study appointment, x-rays and a 3D intraoral scan will be obtained for the purpose of measuring alveolar volume. The health of the mucosa surrounding the implant and subject satisfaction will be assessed via bleeding upon probing and completion of a brief questionnaire, respectively.


Clinical Trial Description

An alveolar ridge is the part of the jawbone which immediately surrounds and anchors the tooth socket ("alveolus"). Similar to any bone or muscle atrophying when not used, the alveolar ridge will shrink ("resorb") following tooth extraction. The volume of an alveolar ridge can be measured by both 3 Dimensional ("3D") intraoral scan and radiography, and is used clinically as a metric of oral health. A dental implant is a medical-grade titanium screw placed into healed alveolar bone or a tooth socket following tooth extraction. It replaces the tooth root and supports the crown, or "dental cap"; an artificial tooth generally made with porcelain or surgical grade metals. Implant success requires both sufficient bone alveolar volume and sufficient mucosal tissue to protect against biofilm-mediated inflammation, assure functional comfort and contribute to dental implant esthetics. Following dental implant placement, the alveolar ridge resorbs approximately 0.5 to 1.0 mm during the first year. Healed ridges are also often volumetrically deficient, losing up to 30% of their horizontal volume following tooth extraction. To remedy this, peri-implant mucosal grafting has been proposed and is currently part of dental implant therapy. Both autogenous grafts (mucosal connective tissue from the roof of the patient's own mouth or "palate") and allogeneic grafts (collagen-rich grafts derived from a genetically non-identical human donor) are used for these purposes, but there is controversy regarding the effectiveness of supplemental graft use during implant treatment. The purpose of this study is to prospectively evaluate whether including an allogeneic gum graft (PerioDerm*) during dental implant therapy improves implant health and appearance. On the day of implant surgery, participating subjects will be randomized to either receive or not receive a supplemental gum allograft along with the implant. Participating subjects will also be asked to complete a brief (about 15 questions) oral health questionnaire. Participating subjects will return to the clinic about 8 weeks post surgery for digital crown impressions and again at 11-13 weeks after surgery for crown placement. Participating subjects will also return to clinic about 1 year after implant placement for assessment of the implant evaluation. At this final study appointment, x-rays, a 3D intraoral scan and intraoral photographs of the implant will be obtained for the purpose of measuring alveolar volume. The health of the mucosa surrounding the implant and subject satisfaction will be measured via bleeding upon probing and completion of a brief questionnaire, respectively. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04082143
Study type Interventional
Source University of Illinois at Chicago
Contact
Status Completed
Phase Phase 3
Start date August 25, 2019
Completion date December 20, 2022

See also
  Status Clinical Trial Phase
Recruiting NCT03459547 - Soft Peri-implant Tissue Around Different Abutment Materials N/A
Completed NCT05724706 - An Evaluation of Salivary Oxidant and Antioxidant Levels in Peri-implant Health and Disease
Completed NCT05494476 - Stability of the Marginal Bone Around Subcrestal Implants N/A
Completed NCT02625597 - Assessment of the Effects of Different Implant Abutment Occluding Materials on Dental Implant Health Parameters and Microbiology N/A
Active, not recruiting NCT03982615 - Impact of Laser-modified Abutment Topography on Peri-implant Mucosal Integration N/A
Completed NCT03501199 - Comparison of Different Materials Contribution to Implants Stability N/A
Recruiting NCT05924711 - "Association of Peri-implantitis and Maxillary Sinusitis: a Case-control Study".
Not yet recruiting NCT04299386 - Effect of Nanocrystal Gels on the Management of Peri-implant Diseases N/A
Recruiting NCT03524872 - Implant/Abutment Module Stability of Original vs Compatible Connections N/A
Completed NCT03041584 - Dental Implants Placed by Using a Drill Guide Versus Non-guided Placement. Follow-up Study N/A
Recruiting NCT04906161 - Vitamin D and Serum Calcium Level Insufficiency and Early Dental Implant Failure
Not yet recruiting NCT05156294 - Effect of Soft Tissue Augmentation With an Acellular Dermal Matrix in Marginal Bone Levels Around Implants Phase 3
Active, not recruiting NCT05595772 - Comparison of Two Different Types of Platelet Concentrate to Augment Bone Around Immediate Dental Implant N/A
Recruiting NCT06135506 - Artificial Intelligence/Computer Guided Ridge Splitting for Treating Horizontal Ridge Defects N/A
Completed NCT06131541 - Ridge Splitting With Implant Placement Using Autogenous Tooth Graft N/A