Factors Affecting Immediate Anterior Implants Esthetics.

NCT07539168 | Not Yet Recruiting DMC

• 1 other identifier: IDCE-31042026
• Study Type: observational
• Target: 500
• Locations: 0 countries
• Sites: N/A

Brief Summary

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).

Conditions

Pink Esthetic Score; Implant Survival Rate; Immediate Implant Placement

Keywords

Immediate implant, esthetics, anterior maxilla

Outcome Measures

Primary Outcomes (1)

• Pink esthetic score

  3 years

Study Arms (1)

IIP in anterior maxilla

Immediate implant placement from canine to canine

Eligibility Criteria

• Age: 21 Years - 55 Years
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64)
• Sampling Method: Probability Sample

Study Population

All patients were treated with flapless immediate implants with no grafting procedures in the esthetic zone.

You may qualify if:

• 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
• patients who had provided an informed consent.

You may not qualify if:

• 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.

Sponsors & Collaborators

• International Dental Contiuing Education: lead

Central Study Contacts

Nourhan Gamal, MSc

CONTACT

+201064249441; Nourhannegamal259@gmail.com

Study Design

• Study Type: observational
• Observational Model: COHORT
• Time Perspective: RETROSPECTIVE
• Sponsor Type: NETWORK
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: Executive Director

Study Record Dates

• First Submitted: April 13, 2026
• First Posted: April 20, 2026
• Study Start (Estimated): June 1, 2026
• Primary Completion (Estimated): August 1, 2026
• Study Completion (Estimated): September 1, 2026
• Last Updated: April 22, 2026

Record last verified: 2026-04

Data Sharing

• IPD Sharing: Will not share