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New treatment option for Bone Resorption
Official title Timing of Soft Tissue Grafting Following Immediate Implant Placement
ClinicalTrials.gov ID: NCT05537545
What this study is testing
- What it's testing
- Patients undergoing single immediate implant placement (IIP) in the premaxilla will be invited to participate in this randomized controlled trial (RCT). Prior to surgery, a small- field low-dose cone beam computed tomography (CBCT) is taken to verify the integrity of the facial bone wall and an adequate amount of apical and palatal bone availability for implant anchorage.
- Which group you join is decided by chance.
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% (O'Leary et al. 1972)
- Presence of an incisor, cuspid or premolar in the maxilla that needs to be extracted for any reason with at least one neighboring tooth present
- At least 3 mm bone available at the apical or palatal aspect of the alveolus as assessed on CBCT to ensure primary implant stability
- Intact buccal bone wall at the time of extraction
You likely can't join if
- Pregnancy
- Systemic diseases
- Smoking
- Suppuration
- \> 1 mm gingival asymmetry between the failing and contralateral tooth
- Untreated periodontal disease; untreated caries lesions
See the full eligibility criteria
- At least 20 years old
- Good oral hygiene defined as full-mouth plaque score ≤ 25% (O'Leary et al. 1972)
- Presence of an incisor, cuspid or premolar in the maxilla that needs to be extracted for any reason with at least one neighboring tooth present
- At least 3 mm bone available at the apical or palatal aspect of the alveolus as assessed on CBCT to ensure primary implant stability
- Intact buccal bone wall at the time of extraction
- Written informed consent
- Pregnancy
- Systemic diseases
- Smoking
- Suppuration
- \> 1 mm gingival asymmetry between the failing and contralateral tooth
- Untreated periodontal disease; untreated caries lesions
The study team makes the final eligibility decision.
Where it's taking place
- Ghent, Oost-Vlaanderen, 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 listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to 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, Oost-Vlaanderen, 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.