Evaluation of biomimetic abutments for dental implants
Research on the Development and Clinical Evaluation of Biomimetic Abutments
This study tests if using special healing and prosthetic parts for dental implants can improve healing and overall results for patients getting dental restorations.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 30 (estimated) |
| Ages | 25 Years to 65 Years |
| Sex | All |
| Sponsor | Stomatological Hospital Affiliated with Fujian Medical University Academic / other |
| Locations | 1 site (Fuzhou, Fujian) |
| Trial ID | NCT06870955 on ClinicalTrials.gov |
What this trial studies
This study evaluates the clinical effectiveness of biomimetic abutments used in dental implant restoration. During the second-stage surgery, biomimetic healing abutments are placed, followed by the use of biomimetic prosthetic abutments to complete the restoration. The study assesses soft tissue changes through digital models collected at various time points and analyzes hard tissue through periapical radiographs. Clinical conditions such as food impaction and plaque index are also monitored throughout the study.
Who should consider this trial
Good fit: Ideal candidates are adults aged 25 to 65 with a single edentulous site and good treatment compliance.
Not a fit: Patients requiring soft tissue grafting, those with severe periodontal issues, heavy smokers, or poor oral hygiene may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could improve the outcomes of dental implant restorations by enhancing soft and hard tissue integration.
How similar studies have performed: While the use of biomimetic materials in dental applications is gaining interest, this specific approach is relatively novel and has not been extensively tested in prior studies.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * aged between 25 and 65 years old * had one single edentulous site * implant embedded healed and required secondary surgery to expose * good treatment compliance and could attend follow-up appointment regularly Exclusion Criteria: * soft tissue grafting was needed * severe acute or chronic periodontitis * heavy smoking habit (\> 10 cigarettes/day) * poor oral hygiene
Where this trial is running
Fuzhou, Fujian
- The Affiliated Stomatological Hospital of Fujian Medical University — Fuzhou, Fujian, China (Recruiting)
Study contacts
- Principal investigator: Hui Cheng, PhD — Stomatological Hospital Affiliated with Fujian Medical University
- Study coordinator: Hui Cheng, PhD
- Email: ch_fujian@163.com
- Phone: 18960883888
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.