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New treatment option for Dental Implants, Single-Tooth
Official title Effect of Abutment Configuration on Peri-implant Soft and Hard Tissue in the Esthetic Zone - Randomized Clinical Trial
ClinicalTrials.gov ID: NCT06407271
What this study is testing
- What it's testing
- The aims of our study are to investigate in patients with immediate implantation replacing a single tooth in the maxillary anterior (#FDI 15-25) region the effect of (a) custom vs cylindrical stock healing abutments, then (b) screw retained single ceramic crowns, on the peri implant hard- and soft-tissue formation and blood flow.
- 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 18 and older. Healthy volunteers may be eligible.
You may be able to join if
- patients over 18 years
- good general health
- good oral hygiene (FMPS \< 25%)
- healthy periodontium (PPD \< 4mm)
- thick phenotype
You likely can't join if
- general ill health
- general surgical or oral surgery contraindication
- a patient who has undergone local radiotherapy
- active periodontal inflammation, inflammation of the alveolar cavity
- smoking
- posterior region
See the full eligibility criteria
- patients over 18 years
- good general health
- good oral hygiene (FMPS \< 25%)
- healthy periodontium (PPD \< 4mm)
- thick phenotype
- maxilla anterior region (extended to 15-25 positions)
- solo missing teeth, intact adjacent teeth
- type 1 alveolar shape after extraction 1
- retained occlusion
- baseline buccal bone wall thickness at least 1.5 mm, based on intact CBCT scan
- patient voluntarily accepts and signs the information and consent form for the study
- general ill health
- general surgical or oral surgery contraindication
- a patient who has undergone local radiotherapy
- active periodontal inflammation, inflammation of the alveolar cavity
- smoking
- posterior region
- pregnancy, lactation
- psychological or mental involvement affecting individual plaque control
- presence of an implant adjacent to the planned implant
- inadequate oral hygiene
- need for vertical bone augmentation
- gingival recession
- Inappropriate implant position for screw fixation
- bruxism
The study team makes the final eligibility decision.
Where it's taking place
- Budapest, Pest County, Hungary
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, 18 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 Budapest, Pest County, Hungary. 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.