RECRUITING

Mix of Demineralized Freeze-Dried Bone Allograft and Deproteinized Bovine Bone Mineral: a Possible Solution for Alveolar Ridge Preservation?

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 purpose of the study is to compare a new grafting material for alveolar ridge preservation to a commonly used and well studied material. Alveolar ridge dimensions as well as histology will be compared.

Official Title

Mix of Demineralized Freeze-Dried Bone Allograft and Deproteinized Bovine Bone Mineral: a Possible Solution for Alveolar Ridge Preservation?

Quick Facts

Study Start:2024-01-26
Study Completion:2025-06
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06275789

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. * Patients in good health
  2. * Require the extraction of at least one premolar or molar with future implant placement
  3. * Sufficient keratinized gingiva (equal or more than 2mm prior to extraction),
  4. * No more than 3mm of buccal bone loss
  5. * Flapless extraction possible
  6. * Full mouth plaque index of less than 25%
  1. * Nicotine consumption equivalent to or more than 10 cigarettes per day
  2. * Electronic cigarette usage
  3. * A history of irradiation of head and neck area
  4. * Immunodeficiency disease
  5. * Uncontrolled systemic health problems (hypertension crisis 180/120, hyperthyroidism, diabetes with HbA1c over 7, recent history of stroke, cancer) History of medications that affect bone remodeling process (bisphosphonates, RANK-L inhibitors)
  6. * Previous adverse reaction to the biomaterials used
  7. * Pregnancy/lactation, or those who are trying to become pregnant.
  8. * Active uncontrolled or untreated periodontal disease
  9. * Periapical lesions greater than 1 cm and soft tissue pathology

Contacts and Locations

Study Contact

Andee Goldstein, DMD
CONTACT
7542599445
ag3577@mynsu.nova.edu
Fatemeh Samavatijame, DMD
CONTACT
(734) 546-9018‬
fs724@mynsu.nova.edu

Study Locations (Sites)

Nova Southeastern University
Fort Lauderdale, Florida, 33328
United States

Collaborators and Investigators

Sponsor: Nova Southeastern 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 Date2024-01-26
Study Completion Date2025-06

Study Record Updates

Study Start Date2024-01-26
Study Completion Date2025-06

Terms related to this study

Additional Relevant MeSH Terms

  • Alveolar Ridge Preservation
  • Dental Extraction
  • Bone Graft