Performance and Safety of Lyoplant® in Guided Bone Regeneration (GBR) in Oral Surgery

NCT06732167 | Recruiting

• 1 other identifier: AAG-G-H-2014
• Study Type: interventional
• Target: 68
• Locations: 1 country
• Sites: 2

Brief Summary

Guided Bone Regeneration (GBR) is a well-established surgical technique that employs barrier membranes to ensure the stability of bone augmentation material while preventing the infiltration of soft tissue, thereby facilitating new bone formation. The primary objective of this randomized controlled trial is to assess the performance and safety of the Lyoplant® collagen membrane as a barrier membrane in GBR for patients undergoing dental implant surgery. Additionally, the study aims to compare the Lyoplant® membrane with the Bio-Gide® collagen membrane, with the goal of demonstrating the non-inferiority of the Lyoplant® membrane in terms of radiographically measured bone gain compared to the comparator.

Conditions

Bone Regeneration

Keywords

collagen barrier membrane

Outcome Measures

Primary Outcomes (1)

• Gain of horizontal bone thickness at the augmented site

  At Visit 2 (V2) and Visit 5 (V5) a Cone Beam Computed Tomography (CBCT) is taken. CBCTs are compared and horizontal bone dimensions at augmented site are measured at four levels (at implant shoulder, 2 mm, 4 mm, and 6 mm from the implant shoulder).

  At Visit 5: 5 months after GBR intervention

Secondary Outcomes (3)

• Number of side effects

  At each follow-up visit: V3 (after 7-14 days), V4 (after 1 month ± 7 days) and V5 (after 5 months ± 2 weeks)

• Number of safety endpoints

  At each follow-up visit: V3 (after 7-14 days), V4 (after 1 month ± 7 days) and V5 (after 5 months ± 2 weeks)

• Membrane usability

  At V2 (surgery): directly after GBR intervention

Study Arms (2)

Lyoplant®

EXPERIMENTAL

Procedure: GBR Lyoplant

Bio-Gide®

ACTIVE COMPARATOR

Procedure: GBR Bio-Gide

Interventions

GBR Lyoplant PROCEDURE

GBR surgical procedure with simultaneous implant placement including membrane placement

Lyoplant®

GBR Bio-Gide PROCEDURE

GBR surgical procedure with simultaneous implant placement including membrane placement

Bio-Gide®

Eligibility Criteria

• Age: 18 Years+
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Patients who are willing to give a voluntary consent to participate in the study, following a full explanation of the nature and purpose of the study, by signing the Informed Consent Form (ICF).
• Patients with the capacity to consent for themselves.
• Patients in need of an implant with a simultaneous GBR procedure.
• Presence of buccal bony dehiscence with a vertical defect height (VDH) ≥ 1 mm and ≤ 6 mm after implant placing.
• The tooth at the implant site must have been extracted or lost at least 8 weeks before the date of bone augmentation (volumetrically healed site).

You may not qualify if:

• Patients \< 18 years.
• Currently pregnant or breastfeeding women.
• Major systemic diseases (e.g. recent myocardial infarction, cerebrovascular accident or valvular prosthesis surgery, a poorly stabilized diabetes mellitus, severe hypertension, severe peripheral artery occlusive disease, malignancies, autoimmune diseases, or kidney diseases, untreated or uncontrolled periodontal disease, uncontrolled drug or alcohol abuse, uncontrolled psychiatric disorders).
• Acute infectious diseases.
• Immunocompromised patients.
• Serious disturbances of bone metabolism and/or serious bone diseases of endocrine etiology.
• Medical conditions requiring prolonged use (\> 6 months) of steroids and/or ongoing treatment with gluco- and mineralocorticoids and with agents affecting calcium metabolism (e.g. calcitonin), and/or anticoagulative therapy.
• Previous or current use of antiresorptive drugs (ARDs) (e.g. bisphosphonates, selective estrogen receptor modulators (SERMs), denosumab, hormone replacement therapy and calcitonin).
• Previous oral / maxillofacial radiotherapy.
• Heavy smoker (\>10 cigarettes/day). In the case of vapors with nicotine, the use of \>300 puff vapors (equivalent to 10 cigarettes/day) are not allowed.
• Health conditions, which do not permit the surgical treatment.
• Use of the Investigational Device / Comparator in infected areas.
• Known foreign body sensitivity to implant materials.
• Simultaneous participation in another interventional clinical trial (drugs or medical devices studies) if it could impact the result of the study.

Sponsors & Collaborators

• Aesculap AG: lead

Study Sites (2)

Hospital Odontològic Universitat de Barcelona, Campus Ciències de la Salut de Bellvitge

Barcelona, Catalonia, 08907, Spain

RECRUITING

Clínica Universitaria d.Odontologia de la Universitat Internacional de Catalunya

Sant Cugat Del Vallés, Catalonia, 08195, Spain

RECRUITING

Central Study Contacts

Izabela Firkowska-Boden, Dr.

CONTACT

+49 7461 95; studies@aesculap.de

Tobias Weber, Dr.

CONTACT

+49 7461 95; studies@aesculap.de

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: RANDOMIZED
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: PARALLEL
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: December 9, 2024
• First Posted: December 13, 2024
• Study Start: January 24, 2025
• Primary Completion (Estimated): June 1, 2026
• Study Completion (Estimated): December 1, 2026
• Last Updated: February 27, 2026

Record last verified: 2026-02

Locations

ES (2)