RECRUITING

Auto Transplantation of Wisdom Teeth

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

Autotransplantation emerges as a viable alternative to tooth extraction and prosthetic restoration when conventional endodontic treatments are unfeasible or contraindicated. The success of autotransplantation is influenced by diverse factors, including root development stage, tooth morphology, surgical technique, extraoral duration, recipient socket shape, recipient bed vascularity, and periodontal ligament cell vitality. Preserving periodontal ligament quality and achieving tissue adaptation are pivotal for successful tooth transplantation. Successful donor tooth replacement is influenced by variables like fitting attempts, alveolus-root distance, extra-alveolar time, surgical skill, and extraction trauma intensity.

Official Title

Auto Transplantation of Wisdom Teeth With or Without Platelet Rich Fibrin for Replacement of Non-Restorable Posterior Teeth.

Quick Facts

Study Start:2024-01-01
Study Completion:2025-03-31
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06553300

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 50 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:ADULT
Inclusion CriteriaExclusion Criteria
  1. * male and female
  2. * aged between 20 and 50 years
  3. * devoid of systemic ailments
  4. * complying with the study procedures
  5. * holding an Anesthesiologists classification of 1 or 2
  6. * possessing mandibular or maxillary immature wisdom teeth
  1. * systemic diseases that might impede the healing process
  2. * Patients with pacemakers
  3. * Individuals harboring allergies to medications or antibiotics
  4. * active smokers
  5. * patients afflicted with periodontal diseases

Contacts and Locations

Study Contact

Luis M De la Rosa, DDS
CONTACT
917-861-5881
l.delarosa@cdiohio.org
Nelza Baladi, DDS
CONTACT
n.baladi@cdiohio.org

Principal Investigator

Waleed Elmallah, DDS
STUDY_CHAIR
Cleveland Dental
Ahmed Hashem, DDS
STUDY_DIRECTOR
Cleveland Dental

Study Locations (Sites)

Cleveland Dental Institute
Cleveland, Ohio, 44128
United States

Collaborators and Investigators

Sponsor: Cleveland Dental Institute

  • Waleed Elmallah, DDS, STUDY_CHAIR, Cleveland Dental
  • Ahmed Hashem, DDS, STUDY_DIRECTOR, Cleveland Dental

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 Date2024-01-01
Study Completion Date2025-03-31

Study Record Updates

Study Start Date2024-01-01
Study Completion Date2025-03-31

Terms related to this study

Additional Relevant MeSH Terms

  • Autotransplantation of Wisdom Teeth
  • Patelet Rich Fibrin