Clinical Trials Logo

Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT06312384
Other study ID # A04080622
Secondary ID
Status Active, not recruiting
Phase Phase 3
First received
Last updated
Start date July 1, 2022
Est. completion date June 2024

Study information

Verified date December 2023
Source Mansoura University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Evaluate the impact of using 3D surgical template with guided bone regeneration technique on the contour of bone augmentation in patients with horizontal labial ridge defect and simultaneous implantation.


Description:

Because adequate bone wrapping around the implant is critical for long-term effectiveness of dental implant treatment, bone augmentation in the bone defect area is required to repair the width and height of the alveolar bone, as bone resorption occurs following tooth extraction. Many bone augmentation techniques, such as onlay block grafting, bone splitting, distraction osteogenesis, and guided bone regeneration, are currently accessible in clinics (GBR). Surgical options vary depending on the severity of the bone deformity. GBR is a bone augmentation technique that has more evidence-based medicine support and therapeutic applications, as well as the benefits of less surgical stress and low technical sensitivity. Establishing aesthetics and guaranteeing long-term success in implant therapy can be challenging. Long-term stable implant success has been linked to the presence of more than 2mm labial graft thickness, and appropriate labial graft thickness is essential to preserve crestal bone level and prevent marginal soft tissue recession. According to a meta-analysis of 15 randomized-controlled trials, the estimated mean (SD) bone resorption for GBR in lateral ridge augmentation throughout the 6-month healing period was 1.22-0.28 mm. As a result, a 3.5 mm thickness of labial graft at all levels may be necessary following wound closure to compensate for potential graft loss. Traditional bone augmentation is often dependent on the operator's skill, therefore virtually digital guided bone regeneration (GBR) process offers the digital options for precise and controllable bone augmentation in the field of oral implantology . Specific aim: to compare the contour of bone augmentation (peri-implant bone volume) between various (GBR) procedures in patients with lateral alveolar ridge defect and simultaneous implantation. Hypothesis: patients with lateral alveolar ridge defect and simultaneous implantation subjected to a 3D printing surgical template with GBR are associated with radiographic evidence of more labial graft thickness and volume stability after six months post-surgical than patients with conventional GBR protocol.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 20
Est. completion date June 2024
Est. primary completion date May 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria: 1. Healthy patients between the ages of 18 and 65 with edentulous ridge and seek for implant replacement. 2. In the anterior region, there is a labial bone defect. 3. Patients need the surgery in the first place to compensate for bone loss around implant. Exclusion Criteria: 1. Systemic disorders that are out of control. 2. Heavy smokers (those who smoke more than 20 per day). 3. Women who are pregnant or nursing. 4. Thin gingival bio-type.

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
3D Surgical Template on the Contour of Bone Augmentation, in Patient With Labial Alveolar Ridge Defect and Simultaneous Implantation
a two-piece tooth-supported surgical template will fabricated through 3D printing technology before surgery base on the digital simulation of bone graft contour.Sticky bone will placed into the defect under the guidance of the template to form customized sticky bone and will be covered with collagen membrane.
conventional guided bone regeneration,in Patient With Labial Alveolar Ridge Defect and Simultaneous Implantation
The defected site will be grafted with sticky bone (particulate bone substitute mixed with injectable platelet-rich fibrin (i-PRF)) and will be covered with collagen membrane.

Locations

Country Name City State
Egypt Faculty of Dentistry-Mansoura University Mansoura

Sponsors (1)

Lead Sponsor Collaborator
Mansoura University

Country where clinical trial is conducted

Egypt, 

References & Publications (1)

Wang M, Zhang X, Li Y, Mo A. The Influence of Different Guided Bone Regeneration Procedures on the Contour of Bone Graft after Wound Closure: A Retrospective Cohort Study. Materials (Basel). 2021 Jan 27;14(3):583. doi: 10.3390/ma14030583. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Change in Radiographic assessment for all patients underwent Cone beam computed tomography (CBCT) scans The postoperative CBCT DICOM images were converted to STL files and overlaid over the preoperative CBCT.The thickness of the labial bone graft was measured from the labial outline of the bone graft to the implant as a result of the procedure. (T0-T5) Perpendicular to the simulated implant in the bucco-oral cross-sectional picture. The distance (width in millimeter) between the implant and the labial contour of the graft, which indicated the thickness of the labial bone graft, was measured at the implant shoulder (T0), as well as at 1, 2, 3, 4, and 5 mm apical to the implant shoulder (T1-T5).
For each site, the standard deviation of T0, T1, and T2 (SDC) was calculated, which represents the uniformity of the graft contour in the coronal area.
baseline, immediately after and 6 months after surgery
See also
  Status Clinical Trial Phase
Completed NCT03076138 - Gene-activated Bone Substitute for Maxillofacial Bone Regeneration N/A
Recruiting NCT03570606 - Clinical Study of Bone Graft Substitutes in Orthopaedic and Spinal Applications.
Completed NCT01738113 - Open Versus Closed Kinetic Chain Exercises in Tibial Distraction Osteogenesis by Ilizarov's METHOD Phase 2
Not yet recruiting NCT05676905 - Prospective Multicenter Observational Study on the Use of NEOCEMENT® for the Treatment of Bone Defects
Active, not recruiting NCT05659069 - Influence of Mandibular Nerve Lateralization on Nutrition and Speech
Recruiting NCT05758623 - Mg-containing Biodegradable Polymer Bone Repair Material N/A