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New treatment option for Dental Implantation
Official title Immediate Implant Placement in the Posterior Region Combining Sealing Socket Abutment and Peri-implant Socket Filling.
ClinicalTrials.gov ID: NCT05741749
What this study is testing
- What it's testing
- The primary endpoint of this study is to compare the soft tissue contour changes after immediate implant placement combined to peri-implant socket filling with a sealing socket abutment (SSA) versus a standard healing abutment. The hypothesis is that the SSA better preserves the alveolar ridge profile in the cervical region compared to a conventional healing abutment.
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 18 to 99. Healthy volunteers may be eligible.
You may be able to join if
- Good general health (ASA I/II),
- More than 18 years old,
- Smoker \< 10c/day, one hopeless tooth,
- Healthy periodontal condition,
- Presence of at least 2 mm of keratinized gingiva
You likely can't join if
- Auto-immune disease or immunocompromised patients
- Uncontrolled diabetes
- Use of steroids or biphosphonates
- Local or systemic infection (medical treatment needed prior to entrance to the study)
- Pregnancy or breastfeeding
- Alcoholism or chronically drug abuse
See the full eligibility criteria
- Good general health (ASA I/II),
- More than 18 years old,
- Smoker \< 10c/day, one hopeless tooth,
- Healthy periodontal condition,
- Presence of at least 2 mm of keratinized gingiva
- Intact buccal bone wall
- Adequate plaque control (FMPS ≤ 25%)
- Adequate bone quantity allowing an immediate implant procedure (apical bone height of at - Least 5 mm or presence of interradicular septum)
- Written consent provided
- Auto-immune disease or immunocompromised patients
- Uncontrolled diabetes
- Use of steroids or biphosphonates
- Local or systemic infection (medical treatment needed prior to entrance to the study)
- Pregnancy or breastfeeding
- Alcoholism or chronically drug abuse
- Bone availability requiring an angulated abutment
- Untreated local inflammation
- Cyst
- Mucosal disease or oral lesions
- Local irradiation therapy
- Oral communication with sinus after the extraction
The study team makes the final eligibility decision.
Where it's taking place
- Liège, 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, 18 years to 99 years. Healthy volunteers may be eligible. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Liège, 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.