Labial Bone Thickness Around Immediate Implants in the Esthetic Zone Following a Novel Socket Evaluation System
NCT06648135
Immediate Implant Placement
Cairo, Egypt
View Trial DetailsNCT Number: NCT07539168
This retrospective cohort study evaluates clinical, surgical, and prosthetic factors associated with early and mid-term outcomes of immediate implant placement in the anterior maxilla. The primary objective is to identify predictors of implant survival and complications (e.g., infection, soft-tissue dehiscence, esthetic failure) within 12 months following placement. Secondary objectives include assessment of peri-implant marginal bone loss, prosthetic complications, and esthetic outcomes (pink esthetic score).
Trial opening soon.
Get Notified21 year–55 year
All sexes
Observational
Study design:
Retrospective observational cohort study using existing patient records and radiographs from IDCE between September 2022 -March 2026. Data extraction will be performed blinded to outcome assessment.
Participants:
Subjects who received immediate implant placement in the anterior region (canine to canine) during the study period with at least 12 months follow-up. Expected sample size: approximately 500 patients/implants
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Time frame: 3 years
Contact information is provided by the study sponsor or research team.
International Dental Contiuing Education
Network
Factors Affecting Immediate Anterior Implants Esthetics . Clinical Retrospective Study
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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