RECRUITING

Comparing Two Surgical Techniques for Building up the Bone Where a Dental Implant is to be Placed

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

The goal of this observational study is to compare two techniques routinely used to increase bone volume in the jaw prior to placing a dental implant, called osseocondensation and osseodensification. The study participants are healthy adults who are planning to get a dental implant. The main questions it aims to answer are: * Is there a difference in wound closure and soft tissue healing following implant placement using osseocondensation versus osseodensification? * Is there a difference in bone density around implants placed with osseocondensation versus osseodensification? * Is there a difference in patient experience during surgery and early phases of healing with osseocondensation versus osseodensification? Researchers will compare implant sites where the osseocondensation technique was used to sites where the osseodensification technique was used to see if there are differences in the outcomes. It is important to note that the research study will not affect what treatment the participants get. The choice of which technique to use will be made by the dentist who is treating them, based on their clinical judgement. The researchers will only compare the outcomes for the techniques. For the research study, participants will undergo additional clinical measurements besides those done as the normal post-operative checks, and will fill out questionnaires about their experiences with the procedures. Getting the bone-increasing procedure and getting the dental implant are not part of the research study.

Official Title

Alveolar Ridge Expansion During Indirect Sinus Lift Procedures--A Comparison of Two Surgical Techiques

Quick Facts

Study Start:2023-05-03
Study Completion:2025-06-30
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06871657

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years to 75 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * 18-75 years old
  2. * Systemically healthy
  3. * No contraindications for implant placement surgery
  4. * No chronic sinus problems
  5. * Non-smoker
  6. * Minimum ridge width of 3 mm and ridge height of 5 mm
  1. * need for ENT specialist clearance due to active problems in relation to ear, not, throat related chronic problems
  2. * sufficient bone volume to perform implant placement without ridge augmentation
  3. * Require guided bone regeneration prior to implant placement
  4. * Need to wear a removable temporary restoration during healing

Contacts and Locations

Study Contact

Binnaz Leblebibioglu, DDS, MS, PhD
CONTACT
614-292-0371
leblebicioglu.1@osu.edu

Study Locations (Sites)

The Ohio State University College of Dentistry
Columbus, Ohio, 43210
United States

Collaborators and Investigators

Sponsor: Ohio State University

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2023-05-03
Study Completion Date2025-06-30

Study Record Updates

Study Start Date2023-05-03
Study Completion Date2025-06-30

Terms related to this study

Additional Relevant MeSH Terms

  • Dental Implant
  • Sinus Floor Augmentation