Marginal Bone Changes in Fixed All-on-Four Mandibular Prosthesis Using OT Bridge Attachment System

Edentulous Jaw Clinical Trial

Official title: Marginal Bone Changes in Fixed All-on-Four Mandibular Prosthesis Using OT Bridge Attachment System Versus Conventionally Screw Retained Multiunit Abutments: A Randomized Clinical Trial

Status Not yet recruiting

Clinical Trial Summary

Group I (control) Edentulous mandible receiving all on four fixed mandibular prosthesis using conventionally screw retained multiunit abutments. Group II (intervention) Edentulous mandible receiving all on four fixed prostheses using OT bridge attachments system. For both groups, the implant sites will be prepared aided by the surgical template. 4 implants with length 11-13 mm will be placed, two anterior implants will be aligned in an axial orientation and two posterior implants will be distally aligned according to the all-on-four concept in the inter foraminal area. Implants will be ideally placed at bone level. For both groups: After implant placement and surgical guide removal, healing abutments ( will be connected during healing periods (eight to twelve weeks). Group I ( control) After eight to twelve weeks from implant placement, multiunit abutments with appropriate heights and angulations will be connected to the implants. Group II ( intervention) After eight to twelve weeks from implant placement, narrow- and low-profile OT Equator abutment will be screwed onto the implants according to the manufacturer. marginal bone changes and prosthetic complications are the outcomes Radiographic follow up will be performed for marginal bone changes Serial of standardized digital periapical radiographs using will be taken at the time fixed prosthesis insertion (baseline), 3,6,9,12 months. Type and incidence of prosthetic complications for the prothesis for each group will be evaluated in 3, 6,9 and 12 months, these complications included: loosening or fracture of the prosthetic screw, prosthesis mobility and fracture of the prosthesis.

Clinical Trial Description

Interventions will be conducted by principal investigator (N.O) General operative procedures: Eligible patients will be selected from outpatient clinic in prosthodontic department clinic. Patients Will be informed of the research work and informed consent will be obtained from each patient. Only motivated patients who show cooperation and has all the included criteria will be into the study. Group I (Control): Edentulous mandible receiving all on four fixed mandibular prosthesis using conventionally screw retained multiunit abutments. Group II (intervention): Edentulous mandible receiving all on four fixed prostheses using OT bridge attachments system. For both groups, a lower removable complete denture will be constructed for each eligible patient. The lower denture will be duplicated into clear acrylic resin which will be modified with radiopaque markers at the proposed implant sites. This clear stent will function as the scan appliance for CBCT scan for detecting the bone high and width, and for implant planning. Surgical phase: All patients in both groups will receive prophylactic antibiotic therapy: 2 g of amoxicillin (or clindamycin 600 mg if allergic to penicillin) 1 h before the intervention and rinse with chlorhexidine mouthwash 0.2% for one minute prior to the intervention. The implants will be placed with a fully surgical guided template, under local anesthesia (artcaine with adrenaline 1:100,000), and according to the manufacturer's instructions. For both groups, the implant sites will be prepared aided by the surgical template. 4 implants (Neobiotech Co., Ltd, Korea) with length 11-13mm will be placed, two anterior implants will be aligned in an axial orientation and two posterior implants will be distally aligned according to the all-on-four concept in the inter foraminal area. The standard sequence of the osteotomy site preparation will be followed to accommodate the selected implant size. Implants will be ideally placed at bone level. Page 12 of 22 Group I: After implant placement and surgical guide removal, screwed healing abutments ((Neobiotech Co., Ltd, Korea) will be connected during healing periods (eight to twelve weeks). Group II: After implant placement and surgical guide removal, screwed healing abutments of (Rhien'83) will be connected during the healing period (eight to twelve weeks). After the surgical procedures end, all the patients will receive drugs prescription, oral and written recommendations about the correct oral hygiene maintenance and diet. Prosthetic phase: Group I: After eight to twelve weeks from implant placement, multiunit abutments (Neo-biotech) with appropriate heights and angulations will be connected to the implants. Impressions will be taken using open tray impression technique for construction of framework superstructure, a posterior cantilever extended to the first molar tooth. The passivity of the metallic framework will be validated intraorally by means of using the single screw test. The non-passive fit will be corrected by sectioning and soldering. The acrylic veneering of the metal superstructure will be made. Group II: After eight to twelve weeks from implant placement, narrow- and low-profile OT Equator abutments (Rhein'83, Bologna, Italy) will be screwed onto the implants according to the manufacturer. The trans-mucosal height of the abutments will be chosen based on the soft tissue thickness and implant depth. Impressions will be taken using open tray impression technique for construction of framework superstructure a posterior cantilever extended to the first molar tooth. the cast framework superstructure splinting all implants will be constructed after placing the acetal rings (Seeger system, Rhein'83) between the subequatorial area of the OT Equators (Rhein'83) and the cylindrical "extra grade" framework connections. Then the prosthesis will be screwed twice at 20 N For both groups, occlusion will be checked using articulating paper for any occlusal interferences, and patients will be enrolled in a strictly follow-up protocol including occlusal adjustment and hygiene maintenance every 3 months. Outcomes: Primary outcome Marginal bone loss will be measured by using periapical X-ray with parallel technique (Digora system), unit of measurment is Millimeter. Prosthetic complications as: 1. Loosening of prosthetic screw 2. Fracture of prosthetic screw 3. Prosthesis fracture These outcomes are Binary and will be measure if incidence of complication happened or not by using (Yes/No). Primary outcome:Radiographic follow up will be performed for marginal bone changes. Serial of standardized digital periapical radiographs using; long cone paralleling technique, XCP periapical film holder and an individually constructed radiographic acrylic template will be taken at the time fixed prosthesis insertion (baseline), 3,6,9,12 months. The software of the Digora system will be used for evaluation of the marginal bone changes. Lines parallel to the long axis of the mesial and distal surface of each abutment will be made. The distance in mm from the crest of alveolar bone to the apex of the tooth will be measured and the marginal bone changes in the subsequent measurements will be calculated. Secondary outcome: Type and incidence of prosthetic complications for the prothesis for each group will be evaluated in 3, 6,9 and 12 months, these complications included: loosening or fracture of the prosthetic screw, prosthesis mobility and fracture of the prosthesis. ;

Related Conditions & MeSH terms

• Edentulous Jaw
• Jaw, Edentulous

• NCT number: NCT05924386
• Study type: Interventional
• Source: Cairo University
• Contact: nesma O elmosallamy
• Phone: 02001007702271
• Email: nesma.osama@dentistry.edu.eg
• Status: Not yet recruiting
• Phase: N/A
• Start date: December 1, 2023
• Completion date: December 31, 2025