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RECRUITING Not applicable ClinicalTrials.gov

Volumetric Efficacy of Alveolar Ridge Preservation

Sponsor: Universidad del Desarrollo • ClinicalTrials.gov ID: NCT07812883

Registry updated: 2026-09-10
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Description

The goal of this clinical trial is to compare the effectiveness of four post-extraction socket management approaches in preserving alveolar ridge dimensions following tooth extraction in adults requiring implant-supported rehabilitation in posterior regions. The main questions it aims to answer are: * Which treatment approach provides the greatest preservation of hard- and soft-tissue dimensions 12 weeks after tooth extraction? * Does the use of a dense polytetrafluoroethylene (d-PTFE) membrane improve alveolar ridge preservation compared with approaches that do not use a membrane? * Are there differences among the treatment groups regarding postoperative healing, complications, pain, and bone regeneration? Researchers will compare spontaneous socket healing, autologous blood clot with d-PTFE membrane, autologous blood clot with leukocyte- and platelet-rich fibrin (L-PRF), and autologous blood clot with L-PRF plus d-PTFE membrane to determine which approach provides the best preservation of alveolar ridge dimensions and tissue healing. Participants will: * Undergo tooth extraction and be randomly assigned to one of four treatment groups. * Receive clinical examinations, intraoral scans, photographs, and cone-beam computed tomography (CBCT) imaging at scheduled follow-up visits. * Complete assessments of postoperative pain and oral health-related quality of life. * Undergo implant placement 12 weeks after tooth extraction, including collection of a bone biopsy for histomorphometric analysis. * Attend follow-up visits to evaluate peri-implant tissue health, marginal bone stability, and implant success up to 24 months after implant loading.

Interventions

  • Spontaneous Healing (Procedure)
    Following atraumatic tooth extraction, the extraction socket is left to heal naturally without the use of alveolar ridge preservation materials, grafting biomaterials, platelet concentrates, or barrier membranes. Healing occurs through spontaneous blood clot formation and physiological post-extraction tissue repair.
  • d-PTFE Membrane (Procedure)
    Following atraumatic tooth extraction, the socket is allowed to fill with an autologous blood clot and is covered with a dense polytetrafluoroethylene (d-PTFE) membrane to protect the socket and support alveolar ridge preservation during healing
  • Leukocyte- and Platelet-Rich Fibrin (L-PRF) (Procedure)
    Autologous leukocyte- and platelet-rich fibrin (L-PRF) prepared from the participant's peripheral blood and placed within the extraction socket to promote tissue healing and support alveolar ridge preservation through the sustained release of growth factors.

Eligibility criteria

Inclusion Criteria: * Adults aged 18 years or older. * Requirement for tooth extraction with the possibility of subsequent implant-supported rehabilitation in the maxillary or mandibular premolar or molar regions. * Extraction sockets classified as Class I to Class Va according to the modified Cardaropoli classification. * American Society of Anesthesiologists (ASA) Physical Status I or II. * Ability to understand the study procedures and provide written informed consent. Exclusion Criteria: * Current treatment with bisphosphonates or systemic corticosteroids. * History of head and neck radiotherapy. * Metabolic bone disorders. * Teeth presenting with acute infectious pathology at the time of extraction. * Pregnancy or breastfeeding. * Inability or unwillingness to attend scheduled follow-up visits. * Any medical or psychological condition that, in the opinion of the investigators, could interfere with study participation or data interpretation.

Conditions

Alveolar Ridge Preservation Tooth Loss Tooth Extraction Tooth Extraction Site Healing Alveolar Ridge Resorption After Extraction

Locations

  • Universidad del Desarrollo (UDD) — Santiago, Santiago Metropolitan, Chile
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Official Source

Data sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.

View Official Record