Evaluating the impact of operator factors on the success of partial indirect dental restorations
Multicenter Prospective Clinical Trial of Partial Ceramic Posterior Restorations Using Immediate Dentin Sealing - The Infuence of Operator Factors on Success and Survival
This study is testing how different techniques used by dentists affect the success and lasting results of certain tooth restorations made from glass ceramics.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 200 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | University Medical Center Groningen Academic / other |
| Locations | 1 site (Groningen) |
| Trial ID | NCT05265559 on ClinicalTrials.gov |
What this trial studies
This observational study aims to assess how different operator factors influence the success and longevity of partial indirect restorations made from glass ceramics. The focus is on the application of immediate dentin sealing (IDS) during the preparation of teeth for these restorations, which are known for their aesthetic quality and high survival rates. By analyzing data from various general practitioners, the study seeks to provide insights into the long-term effects of these treatments in clinical practice. The goal is to enhance understanding of best practices in minimally invasive dentistry.
Who should consider this trial
Good fit: Ideal candidates for this study are healthy adults requiring partial indirect dental restorations.
Not a fit: Patients with unstable periodontal or endodontic conditions, or those with allergies to the materials used, may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved techniques for dental restorations, resulting in better patient outcomes and satisfaction.
How similar studies have performed: While there is limited information on long-term effects from multiple practitioners, the high survival rates of glass ceramic restorations suggest potential for success in similar studies.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Healthy individuals * Adults Exclusion Criteria: * Periodontal unstable situation * Endodontic unstable situation * Allergies for one or more of the used products
Where this trial is running
Groningen
- University Medical Center Groningen — Groningen, Netherlands (Recruiting)
Study contacts
- Study coordinator: M.M.M. Gresnigt, M.D.
- Email: marcogresnigt@yahoo.com
- Phone: +31647494611
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.