ACTIVE_NOT_RECRUITING

Demineralized Bone Allograft Fibers Versus Particulate In Sinus Augmentation

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 this clinical trial is to assess if the addition of DFDBA fibers to DBBM results in greater vital bone formation than the addition of DFDBA particles to DBBM. The study team will examine the effects of the addition of DFDBA fibers to DBBM on vital bone formation. Specifically, we will assess histologically the percent vital bone formation with each of the groups during implant placement, six months after the sinus augmentation procedure. We will also evaluate the radiographic volume achieved with both groups of materials.

Official Title

Demineralized Bone Allograft Fibers Versus Particulate In Sinus Augmentation: A Double Arm Randomized Control And Histomorphometric Study

Quick Facts

Study Start:2023-09-25
Study Completion:2026-05
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:ACTIVE_NOT_RECRUITING

Study ID

NCT06173791

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 89 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Patients between age 18 and 89
  2. * Patients needing sinus augmentation to support implant placement in the posterior maxilla
  3. * Patients must be nonsmokers, former smokers, or current smokers who smoke \<10 cigarettes per day, by self-report
  4. * Female patients who have undergone a hysterectomy, tubal ligation, or menopause, and non- pregnant women of child-bearing potential.
  1. * Patients who disclose that they will not be able to cooperate with the follow-up schedule.
  2. * Patients who are mentally incompetent, prisoners, or pregnant (as obtained via chart review or self-report)
  3. * Pregnant women or women intending to become pregnant during study period
  4. * Smokers who smoke \> 10 cigarettes per day

Contacts and Locations

Principal Investigator

Angela Palaiologou-Gallis, DDS, MS
PRINCIPAL_INVESTIGATOR
The University of Texas Health Science Center at San Antonio

Study Locations (Sites)

University of Texas Health Science Center at San Antonio
San Antonio, Texas, 78229
United States

Collaborators and Investigators

Sponsor: The University of Texas Health Science Center at San Antonio

  • Angela Palaiologou-Gallis, DDS, MS, PRINCIPAL_INVESTIGATOR, The University of Texas Health Science Center at San Antonio

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 Date2023-09-25
Study Completion Date2026-05

Study Record Updates

Study Start Date2023-09-25
Study Completion Date2026-05

Terms related to this study

Keywords Provided by Researchers

  • Tooth loss
  • Bone Resorption
  • Xenograft
  • Allograft

Additional Relevant MeSH Terms

  • Bone Loss in Jaw