Dental Implant Failed Clinical Trial
Official title:
Peri-implant Soft and Hard Tissue Changes Around Maxillary Anterior Immediate Implants Using Socket Shield Technique Versus a Combination of Socket Shield Technique and Autogenous Demineralized Dentin Graft: Randomized Clinical Trial
The current trial aim was to evaluate clinically and radiographically the changes around dental implants inserted immediately in maxillary anterior esthetic zone using a novel combination of autogenous demineralized dentin graft (ADDG) with socket shield technique (SST) and compared this approach to socket shield technique (SST) alone. The present study included 50 participants, aged 20 to 45, with teeth that needed to be extracted. After Kafrelsheikh University research ethics committee approval, participants were randomized into 2 groups: the control group patients underwent immediate implantation using SS protocol, while the study group patients underwent the same procedure, but ADDG was created using the extracted palatal portion of the tooth; and then placed in the peri-implant gap defect.
Status | Recruiting |
Enrollment | 50 |
Est. completion date | July 25, 2024 |
Est. primary completion date | July 17, 2024 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years to 40 Years |
Eligibility | Inclusion Criteria: - above the age of 18years - presence of non-restorable maxillary anterior tooth - had intact socket walls following tooth extraction - the gingival biotype was thick. Exclusion Criteria: - history of systemic condition - history of using bisphosphonates or other drugs that might impact bone turnover - a history of smoking during the previous five years, - a history of any acute infections at the surgical site, - teeth having root resorptions - massive periodontal destruction - buccally fractured root either vertically or horizontally beneath the alveolar crest. |
Country | Name | City | State |
---|---|---|---|
Egypt | oral medicine and periodontology outpatient clinic, faculty of dentistry, kafrelsheikh University | Kafr Ash Shaykh | Kafrelsheikh |
Lead Sponsor | Collaborator |
---|---|
Kafrelsheikh University |
Egypt,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Implant Stability Quotient (ISQ) | Osstell TM was used to record the primary stability.ISQ, or Implant Stability Quotient, is a scale from 1 to 100 and is a measure of the stability of an implant. The ISQ scale has a non-linear correlation to micro mobility. With more than 1400 scientific references, we now know that high stability means >70 ISQ, between 60-69 is medium stability and < 60 ISQ is considered as low stability. | 12-month. | |
Primary | PES | The pink esthetic score (PES) evaluates the esthetic outcome of soft tissue around implant-supported single crowns in the anterior zone by awarding seven points for the mesial and distal papilla, soft-tissue level, soft-tissue contour, soft-tissue color, soft-tissue texture, and alveolar process deficiency.Using a 0-1-2 scoring system, 0 being the lowest, 2 being the highest value, the maximum achievable PES was 14. | 12 months | |
Primary | Midfacial Mucosal Alterations | , digital intraoral scans were recorded. To quantify the vertical changes in the soft tissues around implants buccally, the collected scans were digitally superimposed via matching Gom inspect software | 12 months | |
Secondary | buccal marginal bone level (BMBL) | Utilizing CBCT sagittal sections, the BMBL was evaluated by computerized analysis. Navigation was done on the multiplanar display until the implant's precise same-view location was established on the reformatted cross-sectional section and panoramic view. | 12 months |
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