← Eichor
Study identifier: NCT07080710 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

State of the Art Immediate Implant Placement in the Premaxilla

Condition: Bone Resorption  ·  Sponsor: University Ghent

PhaseNA
Planned participants50
Who can joinAll sexes, 20 Years to no upper limit
Healthy volunteersYes

About this study

The goal of this clinical study is to learn how well immediate implant placement works in the front upper jaw (premaxilla) when using flapless guided surgery, hard and soft tissue augmentation, and immediate provisional crowns. It will also learn about the safety and esthetic results of this treatment approach. The main questions it aims to answer are: Primary: How much buccal bone thickness remains one year after implant placement 1mm below the implant shoulder? Secondary: * How do patients rate pain, healing, and esthetics after treatment? * Are there any complications over the course of five years? * How much buccal bone thickness remains one year after implant placement 3mm and 5mm below the implant shoulder? * Marginal bone loss at one-year and five-year follow-up? * Peri-implant health at one-year and five-year follow-up? * Soft tissue changes at one-year and five-year follow-up? Researchers will compare treatment results in patients with intact bone sockets to those with damaged (non-intact) sockets. Participants will: * Receive a dental implant and temporary crown on the same day as the tooth extraction * Undergo guided, flapless surgery with bone and soft tissue grafting * Take antibiotics and anti-inflammatories for 4 days after surgery * Visit the clinic at 1 week, 3 months, 1 year, and 5 years for follow-up exams * Have X-rays, digital scans, and photos taken to measure bone and soft tissue changes * Answer questions about pain and esthetic satisfaction

This description comes directly from the study's public registry record.

Talk to the study team

Véronique Christiaens, Phd  ·  09/332 40 17  ·  vchristi.christiaens@UGent.be

Jan Cosyn, PhD  ·  09/332 40 18  ·  jan.cosyn@UGent.be

Always discuss trial participation with your own doctor first.

Locations (2)

Ghent UniversityGhent, East Flanders, BelgiumRecruiting
Bv Dr. CosynZottegem, East Flanders, BelgiumRecruiting

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT07080710