Rehabilitation of Single Aesthetic Areas Using Narrow Diameter Implants

Launched by FONDAZIONE POLICLINICO UNIVERSITARIO AGOSTINO GEMELLI IRCCS · Jul 26, 2024

Keywords

ClinConnect Summary

This clinical trial is investigating the use of narrow diameter dental implants to help patients who have lost a single tooth in the front part of their mouth, especially those with less bone thickness or limited space. The goal is to find a simpler and less invasive way to restore these patients' smiles without needing more complicated treatments. While there is not much research on this topic, the trial aims to gather important information about how effective these narrow implants can be.

To participate in this study, you should be an adult over 18 years old, a non-smoker or someone who smokes only a few cigarettes a day, and generally healthy (classified as ASA I or II, which means you have no major health issues). You'll need to sign a consent form to show you understand the study. If you have certain medical conditions, such as severe diseases or uncontrolled diabetes, or if you're pregnant or breastfeeding, you may not be eligible to join. Participants will receive careful follow-up throughout the study to monitor their progress and ensure their safety.

Gender

ALL

Eligibility criteria

• Inclusion Criteria:
• • Patients who have undergone implant surgery to perform implant rehabilitation of single edentulism in the anterior region to insert a reduced diameter implant;
• • ASA I and ASA II patients;
• • Age \> 18yr;
• • Non-smokers or smokers ≤ 5 cig/day;
• • Achievement of FMPS and FMBS ≤ 15%;
• • Signing of the written informed consent to participate in the study.
• Exclusion Criteria:
• • Severe general medical pathologies;
• • Immunodeficiency states;
• • Radiotherapy in the head and neck region;
• • Uncontrolled diabetes or hypertension;
• • Smokers \>5 cigs/day;
• • Impossibility to carry out homogeneous and continuous follow-up;
• • Documented allergy to the biomaterials used;
• • Pregnancy or breastfeeding;
• • Inability to provide written informed consent.