RECRUITING

Alveolar Ridge Preservation With Putty Allograft vs. Putty Alloplast Graft

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Conditions

Alveolar Bone ResorptionAlveolar ridge preservationSocket preservation

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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 primary aims of this study are to compare, after 4 months, the clinical and histologic results of a combination demineralized/mineralized putty allograft vs. synthetic calcium phosphosilicate (CPS) putty alloplast graft utilization in socket preservation procedures. A regenerative tissue matrix membrane will be used to cover each graft lying below the flap.

Official Title

Ridge Preservation Comparing the Clinical and Histologic Healing of Two Different Putty Bone Grafts

Quick Facts

Study Start:2022-10-06
Study Completion:2024-10-30
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT05484492

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
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. 1. Have one non-molar tooth requiring extraction that will be replaced by a dental implant.
  2. 2. Healthy male or female who is at least 18 years old.
  3. 3. Patients must sign an informed consent approved by the University of Louisville Human Studies Committee.
  1. 1. Patients with debilitating systemic diseases, or diseases that have a clinically significant effect on the periodontium.
  2. 2. Presence or history of osteonecrosis of jaws.
  3. 3. Patients who are currently taking IV bisphosphonates or who had IV treatment with bisphosphonates irrespective of duration.
  4. 4. Patients who have been treated with oral bisphosphonates for more than three years.
  5. 5. Patients with an allergy to any material or medication used in the study.
  6. 6. Patients who need prophylactic antibiotics
  7. 7. Previous head and neck radiation therapy.
  8. 8. Chemotherapy in the previous 12 months.
  9. 9. Patients on long term NSAID or steroid therapy.
  10. 10. Pregnant patients.

Contacts and Locations

Study Contact

Bindu Dukka, BDS,MSD,MPH
CONTACT
502-852-1817
himabindu.dukka@louisville.edu
Daniel Ritchey, DMD
CONTACT
513-257-9898
daniel.ritchey@louisville.edu

Principal Investigator

Bindu Dukka, BDS,MSD,MPH
PRINCIPAL_INVESTIGATOR
Director, Graduate Periodontics, University of Louisville

Study Locations (Sites)

University of Louisville
Louisville, Kentucky, 40202
United States

Collaborators and Investigators

Sponsor: University of Louisville

  • Bindu Dukka, BDS,MSD,MPH, PRINCIPAL_INVESTIGATOR, Director, Graduate Periodontics, University of Louisville

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 Date2022-10-06
Study Completion Date2024-10-30

Study Record Updates

Study Start Date2022-10-06
Study Completion Date2024-10-30

Terms related to this study

Keywords Provided by Researchers

  • Alveolar ridge preservation
  • Socket preservation

Additional Relevant MeSH Terms

  • Alveolar Bone Resorption