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Treatment of Mandibular Class II Furcation With Different Types of Biomaterials in Humans

NCT07738705 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 48

Last updated 2026-07-31

No results posted yet for this study

Summary

This randomized controlled clinical trial aims to determine which biomaterial combination yields superior clinical and tomographic outcomes in the treatment of mandibular class II furcation defects. In addition, modifications of gingival phenotype in the furcation area will be assessed.

Conditions

  • Periodontal Furcation Lesions

Interventions

PROCEDURE

Surgical procedure using different types of biomaterials

Compared the results of using different combinations of NovaBone and allograft with a microderm or collagen membranes aiming to decrease or close the furcation lesion.

Sponsors & Collaborators

  • Osteogenics Biomedical

    collaborator INDUSTRY

  • Lake Erie College of Osteopathic Medicine

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-04-18
Primary Completion
2026-07-21
Completion
2026-07-26

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07738705 on ClinicalTrials.gov