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Clinical Trial Summary

The goal of this clinical trial is to compare implant stability, and crestal bone loss, when using minimal invasive ridge splitting versus convenient open flap technique. The main question is Does Minimal Invasive Implant ridge splitting ("transmucosal" without flap) influence the implant stability and crystal bone loss, when compared with the conventional open flap techniques? Researchers will compare Group A: Minimal Invasive Implant ridge splitting and Group B: Triangular flap technique is used to see if there is significant difference between the two groups when measuring implant stability, and crestal bone density.


Clinical Trial Description

Diagnostic stage: Explanation of the operative procedure and obtaining the participants consent. Comprehensive clinical examination and understanding of participants chief complains and needs will be carried out. CBCT acquisition: Cone Beam Computed Tomography (CBCT) scans for the participants will be Taken preoperatively to determine the following: 1. Bone density (D1 & D4 for exclusion, while D2 & D3 shall be included) 2. To confirm the ridge mapping indicating alveolar ridge class IV. (Where height is adequate > 10mm, while width is "3-4 mm"). Planning the surgical procedure: All planned surgical procedure will be carried out by main candidate under supervision. Implant are planned to be placed (2 implants are placed in each segment "30-40 mm") Surgical procedure: Scrubbing and draping of the participants will be carried out in a standard fashion. Local anesthesia (lidocaine 2%o,1/100000 adrenaline) Group A: Minimal Invasive Implant ridge splitting. A horizontal incision is made using fine end bur with high-speed hand piece deep from the edge of the ridge, passing down the cortical plate to the depth of the spongy bone, without mucoperiosteal elevation. Using specially designed implant like bone expanders (Champions implants GmbH) to widen ridge with sequential application (which are 2.4, 2.8, 3.0, 3.3,3.8,4.3, and 5.3 mm in Diameter). With each step the investigators shall carefully check the bone integrity and depth using calibrated probe. By reaching the desired depth and width (till size 3.3 condensers and place 3.5 x 8 mm implants as a standard, using torque gage adjusted at 30-40 Newton's, that's to avoid pressure that might lead to initial resorption. Closure of the incision line using interrupted suturing. Group B: Triangular flap technique is used. With the horizontal component on the ridge and the vertical component posteriorly to avoid injury to the mental nerve, allowed by mucoperiosteal elevation to expose the target area. 2 vertical cuts on both ends to facilitate the ridge expansion, without the risk of crack or fracture of the buccal segment using conventional chisels till reaching the desired width that would accommodate the same implant diameter as for group A. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06329362
Study type Interventional
Source The Royal College of Surgeons of Edinburgh
Contact Bassem Hussein, MDs
Phone +201001113474
Email bassem_26@hotmail.com
Status Recruiting
Phase N/A
Start date July 31, 2023
Completion date July 2025

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