Insertion of Immediate Cortical Satellite Implants With Immediate Loading in the Maxillary Esthetic Zone, a Case Series Study
Trial Snapshot
- Phase
- Not Applicable
- Status
- Not yet recruiting
- Sponsor
- Cairo University
- Enrollment
- 6
- Locations
- 1
- Primary Endpoint
- final implant stability after satellite implant device removal.
Study Overview
Brief Summary
Statement of the problem:
Based on the literature traditional immediate implant with immediate loading has high failure rate due to destructive horizontal forces, accordingly It was recommended for long time stress-free healing periods to achieve the osseointegration of dental implants.
But unfortunately this long time to restore the missing teeth is unsatisfactory to the patient due to high increase of patients' demand for perfect restoring missing teeth preservation of soft and hard tissues with better esthetic and functional results with decreasing the treatment plan time.
Rationale for conducting the research:
This study aimed to add a satellite implant device around the root form implant to enhance the primary implant stability for immediate loading followed by assessment of the final implant stability and final bone quantity and quality around the placed implant
Detailed Description
Research question:
Does the use of satellite implant technique for immediate loading will effectively reduce the treatment time without affection of the final implant stability and the final bone quality and quantity around the placed root form dental implant?
Statement of the problem:
Based on the literature traditional immediate implant with immediate loading has high failure rate due to destructive horizontal forces, accordingly It was recommended for long time stress-free healing periods to achieve the osseointegration of dental implants.
But unfortunately this long time to restore the missing teeth is unsatisfactory to the patient due to high increase of patients' demand for perfect restoring missing teeth preservation of soft and hard tissues with better esthetic and functional results with decreasing the treatment plan time.
Study Design
- Study Type
- Interventional
- Allocation
- Na
- Intervention Model
- Single Group
- Primary Purpose
- Treatment
- Masking
- None
Eligibility Criteria
- Ages
- 18 Years to 60 Years (Adult)
- Sex
- All
- Accepts Healthy Volunteers
- Yes
Inclusion Criteria
- •Patients seeking implant drive prosthesis after immediate extraction technique .
- •Fresh extraction sockets with undestructed labial or palatal walls.
- •Patients with non-restorable teeth due to untreatable caries or trauma.
Exclusion Criteria
- •General contraindications to implant surgery.
- •Active infection or severe inflammation in the area intended for implant placement
- •Teeth non restorable due to periodontal issues.
- •Poor oral hygiene and motivation.
- •Pregnant or nursing.
- •Substance abuse.
- •Psychiatric problems or unrealistic expectations.
- •Severe bruxism or clenching.
- •Immunosuppressed or immunocompromised.
- •Treated or under treatment with intravenous amino-bisphosphonates.
- •Patients participating in other studies, if the present protocol could not be properly followed
Arms & Interventions
subjected to immediate cortical satellite implants with immediate loading
All patients involved in this study will be subjected to immediate cortical satellite implants with immediate loading
Intervention: immediate satellite implant with immediate loading (Device)
Outcomes
Primary Outcomes
final implant stability after satellite implant device removal.
Time Frame: 6 months
OUT COME Calculate the final implant stability after plate removal. MEASURE DEVICE Osstell "resonance frequency analyzer" MEASURE UNIT ISQ
Secondary Outcomes
No secondary outcomes reported
Investigators
Esraa Essam Mohamed Mahmoud
master candidate
Cairo University