Clin2
NCT07879495Possibly a fitNot yet recruiting

Preserving jawbone after tooth removal with synthetic material

Alveolar Ridge AugmentationBone SubstitutesGuided Tissue Regeneration, PeriodontalCone-Beam Computed TomographyBone Resorption

Part of Bones, joints & muscles clinical trials.

This study tests a synthetic bone substitute and a resorbable membrane placed in the tooth socket right after removing a lower premolar or first molar. The goal is to see if this keeps the jawbone and gums healthy for future dental implant placement, using 3D imaging and scans to measure changes over 4 months.

Summary written for real people, not researchers, by Clin2.

Phase
Phase 1/Phase 2
Enrollment
28 people
Ages
18 years and older
Study type
Interventional

Who can take part

  • You are an adult older than 18 and able to understand the study and sign a consent form.
  • You have at least one lower premolar or first molar that cannot be saved and needs to be removed, with plans to get a dental implant later.
  • The bone on the cheek side of that tooth must be intact and at least 1 mm thick, as confirmed by a 3D scan.
  • Your mouth must be free of active infections in the area, including pus, fistulas, abscesses, or large lesions around the tooth root.
  • Your overall gum health must be good, with less than 20% of plaque and less than 20% bleeding on probing.
  • You do not have uncontrolled conditions like diabetes (HbA1c > 7%), are not on medications affecting bone healing (e.g., bisphosphonates), do not smoke more than 10 cigarettes per day, are not pregnant or breastfeeding, and can attend follow-up visits including scans.

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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