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Search / Trial NCT05419778

Alveolar Ridge Preservation Procedures

Launched by UNIVERSITY OF TENNESSEE · Jun 10, 2022

Trial Information

Current as of August 02, 2025

Completed

Keywords

Bone Osteo Gen Cortico Cancellous Foreign Body Reaction

ClinConnect Summary

There will be two(2) groups of standardized treatment (tooth extractions will not take place for research purposes. The Periodontal clinic receives referred tooth extraction indications for treatment as part of the patient's overall treatment plan) evaluated for this study. Subjects will be randomized to either treatment a) standard of care treatment for tooth extraction and ridge augmentation procedures with Cytoplast GRB, or b) standard of the care treatment protocol and ridge augmentation procedures with Osteogen.

Each individual extraction site of the enrolled subject will be randomly ...

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • UT Clinic Participates
  • Participates that live within 100 miles of UTHSC.
  • Participates at least 12 years of age. If participants are 13-14 years of age, the premolars and molars will be included in this study. #2-15 \& #18-31.
  • Participates willing to cooperate with the post-operative instructions;
  • Participates with 2 or more (multiples of 2) teeth needing Maxillary/mandibular and anterior/posterior teeth extractions without restrictions due to the percentage of surface area after the extraction and not interfering with the tooth's alveolar soft tissue exposed surface area.
  • Participates with the availability of returning for 8 visits for data collection.
  • Participants are willing to cooperate with answering the VAS and taking standardized photographs.
  • Participants are physically able to tolerate surgical procedures based on current medical history.
  • Participates able to provide voluntary consent; read and understand English
  • Exclusion Criteria:
  • Participates with Diabetes
  • History of use of bisphosphonates
  • Current smoker
  • If the participant is 12-13 years of age, the tooth/teeth to be removed will not be a primary tooth due to the permanent teeth developing underneath the primary teeth.
  • Pregnant and lactating women

About University Of Tennessee

The University of Tennessee is a leading research institution dedicated to advancing healthcare through innovative clinical trials. With a commitment to improving patient outcomes and fostering scientific discovery, the university engages in a diverse range of studies that encompass various medical disciplines. Leveraging its extensive resources, expert faculty, and state-of-the-art facilities, the University of Tennessee collaborates with healthcare professionals and industry partners to translate research findings into practical applications. Through rigorous ethical standards and a patient-centered approach, the university aims to contribute significantly to the field of medicine and enhance the well-being of communities.

Locations

Memphis, Tennessee, United States

Patients applied

0 patients applied

Trial Officials

Cimara F Ferreira, PhD

Principal Investigator

University of Tennessee

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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