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Purpose: The present study was aimed to evaluate the bone height changes around abutments with two different framework materials for extracoronal attachment mandibular bilateral distally extension removable partial denture (RPD) and compare patient satisfaction associated with its use.
Materials and methods:
Ten partially edentulous patients (long span kennedy class I) were selected, for all patients splinting of remaining abutment were done by porcelain fused to metal bridges, after cementation the RPD frameworks were digitally designed by CAD software and printed into 3-D resin pattern after intra-oral try in of these patterns, the patients were divided into two equalized groups, the patients in first group received extracoronal attachment (RPD)with from milled PEEK (Juvora) framework. While patients in second group received extracoronal attachment (RPD) with conventional metal framework by lost wax technique. Digital radiography was used for bone height assessment of distal abutment at time of prosthesis insertion, 6 and 12 months later. Patient satisfaction was measured using VAS scale.
Full description
I-Patient selection For this study, ten patients (50-60) with mean age 55 years will be selected from out clinic patients Prosthodontic Department, Faculty of Dentistry, Kafr El_Sheikh University. The patients will have the following inclusion criteria:- Completely edentulous maxillary arch against partially edentulous mandible with only remaining mandibular anterior teeth. The selected patients will be free from any systemic diseases, the patients have Angle class I maxillomandibular skeletal relation, the distal extension ridge will be well formed and covered by healthy, firm mucosa, Good abutments with healthy periodontal ligament and suitable crown/root ratio (CRR) as verified by periapical radiograph.
The exclusion criteria to the patients were:
Patients with any systemic disease that could affect the rate of bone resorption which verified by obtaining a medical history, Patients with Para-functional habits (Bruxism and clenching), Patients with any septic foci or impacted teeth as verified by panoramic radiograph, Patients with tilted or rotated abutments. Patients with soft tissue undercuts involved in the design.
For every patient the following procedures were done:
II. Prosthetic procedures:
For each patient, the definitive mandibular extra coronal attachment removable partial denture will be designed using CAD/CAM technology
-Scanning the Master Model The mandibular master cast with porcelain crowns will be then fixed on the scanner table and scanned using the 3D scanner to obtain the standard triangulation file (STL) format.
(Master cast) will be fixed on the table of 3 Shape scanning machine dental system, after application of scan-able spray (Telescan Spray zur vorbereitong von oberflacohen .Teleskop kronen) over the stone teeth and porcelain crowns of master model.
According to the framework material and technique of construction, the patients will be equally divided in to two groups as the following:
Group A: Patients will receive RPD frameworks fabricated from PEEK material using milling machine (CAD/CAM technology).
Group B: Patients will receive RPD frameworks fabricated from Co-Cr material using casting machine.
For group (A) PEEK RPD framework construction will be done as follow:
The virtual 3D framework (STL) file will be sent to the milling machine to begin the milling process of PEEK discs to produce mandibular attachment removable partial denture PEEK framework.
The PEEK framework will be then finished and polished then reseated on the master cast to check its fitting. After that, the PEEK framework will be tried in the patient mouth to check its fitting.
For group (B) metallic RPD framework construction was done as follow:
The virtual 3D framework (STL) file with supporting bars and sprues will be printed with resin and then invested, burnt out, and casted with chromium cobalt alloy to produce mandibular attachment removable partial denture metallic framework.
The metallic RPD framework will be then finished, polished and reseated on the master cast to check its adaptation. After that, the metallic framework will be tried in the patient mouth to check its fitting.
For each patient the in the two groups:
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Inclusion and exclusion criteria
Inclusion Criteria:
The average age of selected patients was from 55 -60 years .
The exclusion criteria to the patients were:
Primary purpose
Allocation
Interventional model
Masking
28 participants in 2 patient groups
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Data sourced from clinicaltrials.gov
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