Bone Substitutes

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Review clinical trials related to Bone Substitutes. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Bone Substitutes and NIPSA in Intrabony Periodontal Defects: A Randomized Controlled Trial

This multicenter randomized controlled clinical trial aims to compare the clinical, radiographic, microbiological and molecular outcomes of two collagenated xenogeneic bone substitutes (GTO® and GenOs®) used in combination with the Non-Incised Papilla Surgical Approach (NIPSA) for the treatment of intrabony periodontal defects. The study will evaluate whether differences exist between the two biomaterials with respect to clinical attachment gain, defect resolution, wound healing and biological markers of regeneration.

Participants needed: 30
Trial details
Age: 18-80Biological sex: AllType: InterventionalSponsor: University of BelgradeUpdated: Jun 26, 2026Locations: 2
Eligibility criteria

Age ≥ 18 years [+5]

Systemic medical contraindications to periodontal surgery [+6]

Status: Not yet recruiting

Bone Augmentation Techniques in the Mandible Posterior Region

This study will compare three methods to rebuild lost bone in the back part of the lower jaw (posterior mandible) before dental implant placement. Seventy-eight adults will be randomly assigned to receive one of three "cortical shell" techniques using either the patient's own bone (autogenous) or prefabricated bone plates from animal (xenogeneic) or human donors (allogeneic). In all groups, the space inside the shell will be filled with a mixture of small bone chips and bone substitute material. The main outcome is the increase in jawbone width measured on 3D cone-beam CT scans at 6 months after surgery. Additional scans and clinical assessments up to 12 months will evaluate healing, bone stability, and postoperative recovery.

Participants needed: 78
Trial details
Age: 18-64Biological sex: AllType: InterventionalSponsor: Universidad de Especialidades Espiritu SantoUpdated: Feb 20, 2026Locations: 1
Eligibility criteria

Not listed

Status: Not yet recruiting

Adjunctive Use of Polynucleotide and Hyaluronic Acid-based Gel in Alveolar Preservation After Tooth Extraction

Alveolar ridge resorption after tooth extraction is a physiological process that continues throughout the patient's life due to the loss of the periodontal ligament and lack of mechanical stimulation. Alveolar ridge preservation (ARP) techniques aim to minimize dimensional changes in the ridge after tooth extraction. These techniques involve grafting the socket to fill the bed and/or sealing it with a biomaterial. Currently, there is a polynucleotide and hyaluronic acid-based gel (Regenfast®) on the market that has proven useful in treating residual periodontal defects. Hyaluronic acid-based gels also appear to enhance the regenerative potential of critical bone defects in both in-vitro studies on rats and clinical studies. Therefore, this study aims to evaluate the clinical and histological effects of polynucleotide and hyaluronic acid-based gel in alveolar preservation procedures.

Participants needed: 20
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Adrià Jorba GarcíaUpdated: Oct 9, 2024Locations: 1
Eligibility criteria

Adults (>18 years) who need the extraction of a single non-molar tooth in the ma... [+3]

Mandibular incisors and molars. [+5]