Dental Implant
Conditions
Keywords
virtual planning;, computer guided implants;, freehand implant;, dental implant
Brief summary
This study's goal is to evaluate the efficacy of traditional rehabilitation with freehand implant implantation of partly or totally edentulous patients utilizing flapless or mini-flap procedures vs. 3D implant design software and specialized surgical templates.
Detailed description
Patients with at least 7 mm of height and 4 mm of breadth in their bones, who needed at least two implants to be restored with a single prosthesis, were recruited one after the other. Patients were randomly assigned to two groups in a parallel group trial design. : Group I: consisted of 6 patients where computer guided dental implant placement and Group II: included six people who had dental implants placed manually. A temporary prosthesis was inserted into the implants right away, and four to six months later, a permanent prosthesis took its place. Implant failures, marginal bone loss, number of therapy sessions, length of treatment, post-surgical pain and swelling, use of painkillers, surgical time, time needed to resolve problems, and patient satisfaction were among the outcome variables evaluated by a blinded, independent assessor. Patients were tracked for a full year.
Interventions
PROCEDUREdental implant
consisted of 6 patients where computer guided dental implant placement
Sponsors
October 6 University
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
40 Years to 65 Years
Healthy volunteers
Yes
Inclusion criteria
* totally edentulous in one or both arches, * with at least 7 mm of height and 4 mm of breadth in their bones as assessed by preoperative CBCT scans. * patients between the ages of 35 and 65 who could give informed permission, * Implants next to each other required to be positioned at least 3 mm apart from each other and 1.5 mm apart from the tooth.
Exclusion criteria
* Patients who have received radiation therapy to the head and neck region within the year prior to implantation, * those who are receiving intravenous amino bisphosphonates, * those who have untreated periodontitis, * those with uncontrolled diabetes, * pregnant women, or nursing mothers are among the general contraindications to implant surgery.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| marginal bone loss | 6 months postoperative | Cone Beam Computed Tomography |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| post-surgical pain and swelling | 7 days prior to implant placement | Visual Analog Scale (10 represent maximum pain , 0 represent no pain) |
Countries
Egypt
Outcome results
None listed