faculty of dentistry , Tanta university
Tanta, Elgharbia, 3111, Egypt
NCT Number: NCT07463469
This study was conducted at the Department of Oral and Maxillofacial Surgery, Faculty of Dentistry, Tanta University. A prospective non-controlled clinical study was performed on ten patients with compromised zygomaticomaxillary bone. Surgical intervention was carried out using a customized surgical guide.
Pre-surgical planning was performed using computed tomography (CT) scans for each patient. Surgical guides were fabricated using direct metal laser sintering technology. Zygomatic implants were inserted using a guided surgical protocol and specialized instruments.
Postoperative CT scans were obtained to evaluate deviations between the planned and actual implant positions. Accuracy was assessed by superimposing the postoperative implant position onto the virtual pre-surgical implant plan using dedicated software. Descriptive and bivariate statistical analyses were performed.
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Notify Me25 year and older
All sexes
Interventional
Not applicable
Tanta, Elgharbia, 3111, Egypt
Purpose: The aim of this study was to evaluate the accuracy of using a static surgical guide protocol for zygomatic implant placement in patients with compromised zygomaticomaxillary bone.
Materials and methods: All the patients had a pre-operative initial consultation interview with the surgeons mainly for collecting demographic data, taking general medical, surgical, and dental history, and listening to the patient's esthetic complaints and postoperative expectations.
Post-operative assessment:
All patients were regularly followed up on the 7th & 14th days postoperatively to assess the following parameters:
Radiographic assessment:
Superimposition
Radiographical evaluation:
Implant Placement Accuracy
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Zygomatic implant placement using a customized bone-supported surgical guide.
Indications included:
Time frame: 3 months
Implant success was assessed based on clinical stability and osseointegration. Stability was evaluated using torque testing during implant uncovering with a torque value of 10-20 Ncm applied to the multiunit abutment screw without implant rotation.
Time frame: 1 year
Implant survival was assessed based on the absence of implant mobility, pain, infection, peri-implant inflammation, suppuration, and progressive bone loss.
Time frame: 1 week
Deviation at the coronal entry point of the implant between the planned implant position and the actual postoperative implant position measured using three-dimensional superimposition of preoperative planning and postoperative CT scans.
Time frame: 1 week
Linear deviation at the apical endpoint of the implant between the planned implant position and the postoperative implant position measured using three-dimensional image superimposition.
Time frame: 1 week
Angular deviation between the long axis of the planned implant and the postoperative implant measured in degrees using 3D software analysis.
Time frame: 4 weeks
Postoperative clinical evaluation of the surgical site including signs of inflammation, infection, or intraoral wound dehiscence.
Time frame: 1 year
Evaluation of prosthetic success including structural integrity of the prosthesis, absence of fracture or wear, and stability of the implant-prosthesis connection.
Time frame: 1 year
Patient-reported outcome measured using the Oral Health Impact Profile-14 questionnaire to assess functional limitation, pain, psychological discomfort, and social disability.
Tanta University
Other
Evaluation of the Accuracy of Three-Dimensionally Guided Zygomatic Implant Placement: A Prospective Clinical Study
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