Evaluation of Interchangeable Guide in Flapless Ridge Splitting With Simultaneous Implant Placement (Clinical Study)
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Anterior Maxillary Narrow Ridge
- Sponsor
- Hams Hamed Abdelrahman
- Enrollment
- 8
- Locations
- 1
- Primary Endpoint
- Postoperative Pain
- Status
- Completed
- Last Updated
- 5 years ago
Overview
Brief Summary
A clinical trial was conducted to evaluate the accuracy of dental implant placement in narrow ridges after ridge splitting flapless technique using an interchangeable guide.
Detailed Description
A sample was selected conveniently to fulfill a list of inclusion and exclusion criteria. Then the selected participants underwent ridge splitting with the aid of interchangeable guide. After ridge splitting, all patients had simultaneous implant placement followed by clinical and radiographical evaluation over a period of 6 months.
Investigators
Hams Hamed Abdelrahman
Assistant lecturer
Alexandria University
Eligibility Criteria
Inclusion Criteria
- •Patients with anterior maxillary narrow ridge
- •Patients with adequate alveolar ridge bone height
- •Age ranging from 20-40 years.
- •Patients should have adequate oral hygiene
- •Patients should be free of soft tissue or oral dental pathology
- •Patients who accept to participate in the study.
Exclusion Criteria
- •Patients suffering from relevant systemic and/or metabolic diseases
- •Patients suffering from immunosuppressive and/or autoimmune diseases
- •Heavy smokers.
Outcomes
Primary Outcomes
Postoperative Pain
Time Frame: After 1 week
Visual Analouge Scale (VAS) 0=no pain 1. mild pain; it is easily tolerated 2. moderate pain; it is causing discomfort but bearable. 3. severe pain; it is causing discomfort, hardly tolerated and unbearable.
Change of bone width from baseline measurements
Time Frame: Baseline, 1 week, 3 months and 6 months
Cone beam computed tomography (CBCT) was used to evaluate bone width and density to all patients by doing CBCT at time intervals
Clinical evaluaion
Time Frame: After 1 week
post operative complication (presence or absence of any sign of swelling or infection)
Secondary Outcomes
- operation time(During the procedure)