Factors Affecting Immediate Anterior Implants Esthetics.
Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age21-55
SponsorInternational Dental Contiuing Education
About this trial
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).
Eligibility criteria
Qualifiers
flapless immediately placed implants in esthetic zone with 3 years follow up CBCT,
presence of immediate postoperative CBCT,
initial intact thick gingival biotype with at least 2 mm band of keratinized tissue
thin intact labial bone plate (< 1mm) extending 7 mm apically assessed by CBCT with good apical bone
Disqualifiers
patients with medical conditions that would compromise the surgical procedures, uncontrolled diabetes mellitus, taking IV bis-phosphonates for treatment of osteoporosis
patients with active infection related at the site of implant and patients with untreated active periodontal diseases.
Trial design
Treatments tested in this trial
- Not listed
Trial groups
500 Participants
are grouped into 1 trial groupLocations
Sponsors and collaborators
Source ClinicalTrials.gov