Alveolar Bone Loss* / Therapy

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Review clinical trials related to Alveolar Bone Loss* / Therapy. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

Clinical Study of BMP-2 Injectable Hydrogel for Promoting Alveolar Bone Regeneration

This project aims to construct an injectable self-healing hydrogel loaded with BMP-2, with optimized gelation time and mechanical strength to meet the requirements for periodontal pocket filling, for the treatment of periodontitis and acceleration of tissue repair, achieving a "bactericidal-anti-inflammatory-regenerative" trinity function. This project will provide a novel intelligent material for promoting alveolar bone regeneration in periodontitis and establish a theoretical paradigm for the precise intervention of oral infectious diseases.

Participants needed: 80
Trial details
Age: 18-70Biological sex: AllType: InterventionalSponsor: The First Affiliated Hospital of Xinxiang Medical CollegeUpdated: May 28, 2026
Eligibility criteria

Clinical Diagnosis: Meets the 2018 International Classification of Periodontal D... [+3]

Systemic Interference with Bone Metabolism: Presence of poorly controlled diabet... [+3]

Status: Not yet recruiting

Study on Silk Fibroin-Reinforced Collagen-Based Composite Membrane for Periodontal Bone Tissue Regeneration

Based on the mechanism of intramembranous ossification of the alveolar bone, it is necessary to design a biomimetic membrane material based on the principle of GBR (Guided Bone Regeneration) to simulate the biological microenvironment of alveolar bone regeneration, promote the direct differentiation of stem cells into osteoblasts and rapid mineralization, thereby achieving the goal of alveolar bone regeneration. This section, based on bionic principles, proposes to enhance the mechanical properties of the collagen membrane with silk fibroin to achieve synergistic regeneration of periodontal bone/soft tissue. This project employs silk fibroin-reinforced collagen membrane technology to overcome the dual bottlenecks of insufficient strength and excessively rapid degradation of existing materials; establishes a "structure-guided, mechanically supported, factor-controlled release" trinity regeneration strategy to achieve precise repair of periodontal composite tissues. This study will provide new materials and methods for periodontal regeneration and offer a theoretical reference for the combined regeneration of other hard/soft tissues.

Participants needed: 80
Trial details
Age: 18-70Biological sex: AllType: InterventionalSponsor: The First Affiliated Hospital of Xinxiang Medical CollegeUpdated: May 8, 2026
Eligibility criteria

Clinical Diagnosis: Meets the 2018 International Classification of Periodontal D... [+3]

Systemic Interference with Bone Metabolism: Presence of poorly controlled diabet... [+3]

Status: Recruiting

Flapless Periodontal Regeneration Using Hyaluronic Acid Versus Enamel Matrix Derivative

The goal of this clinical trial is to radiographically assess the effectiveness of minimally invasive non-surgical technique (MINST) combined with local administration of sodium hypochlorite gel (Perisolv®) and 1.6% cross-linked hyaluronic acid (HA, Hyadent BG®) compared to a neutral formulation of EDTA (Prefgel®) and enamel matrix derivative (EMD, Emdogain® FL) in periodontal regeneration. The main questions it aims to answer are: * ¿Does the combination of MINST with the local administration of sodium hypochlorite gel and 1.6% cross-linked hyaluronic acid show a potential for periodontal regeneration similar to evaluating clinical and radiographic variables compared to a neutral formulation of EDTA and enamel matrix derivative? * ¿What is the patient perception and satisfaction with the received treatment? Researchers will compare A (MINST with Perisolv® + Hyadent BG®), B (MINST with PrefGel® + Emdogain® FL) and C(MINST without any bioactive product). The sample will be distributed according to the following treatments: * Experimental group: Scaling and root planing (SRP), MINST with Perisolv® + Hyadent BG®. * Active comparator group: SRP, MINST with PrefGel® + Emdogain® FL. * Control group: SRP, MINST without any bioactive product. Patients will be screened by a first visit in which they will be assigned their periodontal status. If they meet the eligibility criteria, they will be treated according to the EFP clinical guideline for periodontitis treatment: step I and step II.If the periodontal defect persists at the 12-week re-evaluation, patients will be randomised to treatment A, B or C. After the intervention, all participants will be checked weekly for the first 6 weeks to remove accumulated plaque, and every 3 months for 1 year. Periodontal parameters will be re-evaluated 6 and 12 months after periodontal regenerative intervention.

Participants needed: 60
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: University of ValenciaUpdated: Jan 14, 2026Locations: 1
Eligibility criteria

Periodontitis stage III or IV, grade A or B (Tonetti et al., 2017): attachment l... [+11]

The participant is pregnant, breastfeeding or plans to become pregnant in the ne... [+8]