Recruiting NA Bone Resorption

New treatment option for Bone Resorption

Official title State of the Art Immediate Implant Placement in the Premaxilla

ClinicalTrials.gov ID: NCT07080710

What this study is testing

What it's testing
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.
  • Time commitment: about 1 week

A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.

Who can take part

Ages 20 and older. Healthy volunteers may be eligible.

You may be able to join if

  • At least 20 years old
  • Good oral hygiene defined as full-mouth plaque score ≤ 25%
  • Presence of one or more incisors, cuspids or premolars in the maxilla that need to be extracted for any reason with at least one neighboring tooth...
  • At least 3 mm bone available at the apical or palatal aspect of the alveoli as assessed on a three-dimensional radiograph to ensure primary implant...
  • Written informed consent.

You likely can't join if

  • Pregnancy (will be explicitly asked)
  • Systemic diseases
  • Smoking; suppuration
  • \> 1 mm gingival asymmetry between the failing teeth and contralateral teeth
  • Failing teeth outside the bone envelop as assessed on a three-dimensional radiograph
  • Untreated periodontal disease; untreated caries lesions.

The study team makes the final eligibility decision.

Where it's taking place

  • Ghent, East Flanders, Belgium
  • Zottegem, East Flanders, Belgium

Questions & answers

Do participants get paid in this trial?

This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.

Is it free to join, and do I need insurance?

Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.

How long does this study last?

The study runs about 1 week per participant, based on its public description. The team confirms the exact schedule and number of visits before you enroll.

Who can join this trial?

This study is enrolling all sexes, 20 years and older. Healthy volunteers may be eligible. The study team makes the final eligibility decision.

Where is this trial taking place?

Study sites include Ghent, East Flanders, Belgium; Zottegem, East Flanders, Belgium. Enter your location above to see the nearest site and check your eligibility.

Explore other conditions

BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.