Periodontal Regeneration at the Distal Site of Second Molars After the Extraction of Lower Included Third Molars
NCT ID: NCT07059247
Last Updated: 2025-07-10
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
NOT_YET_RECRUITING
PHASE4
24 participants
INTERVENTIONAL
2025-07-31
2026-09-30
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Among the periodontal considerations regarding impacted third molars, two aspects have traditionally been included: 1)The periodontal damage that certain impactions can cause to the periodontal health of the second molar, and 2) the periodontal sequelae or complications that the extraction of a wisdom tooth may leave on the distal surface of that second molar.
Various therapeutic approaches have been described in the literature to prevent periodontal damage following the surgical intervention involved in the extraction of a fully or partially impacted wisdom tooth. These include scaling of the distal surface of the 2M after extraction, modifications in the surgical technique - such as flap design or suturing method - and various regenerative techniques.
Within this context, the clinical research in which we invite the patients to participate will be developed. We will study the changes in bone levels on the posterior part of the second molar that is in contact with or close to the third molar, as well as the health of the soft tissues, after performing a conventional extraction protocol of the impacted lower third molar. This protocol includes the placement of a regenerative material of porcine origin (test procedure; enamel matrix derivatives) and will be compared to extraction without such material - and therefore without any attempt at periodontal regeneration (standard procedure). The patients will be closely followed up to one year after the surgical performance. This follow-up will be performed clinically and radiographically.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Evaluation of a New Technique for Periodontal Pocket Reduction in the Extraction of Wisdom Teeth
NCT05722509
Impact of Advanced Platelet Rich Fibrin and Enamel Matrix Derivative on Clinical and Molecular Wound Healing Parameters After Surgical Removal of Mandibular Third Molars
NCT06190015
The Efficacy of A-PRF+ on Postoperative Outcomes Following Surgical Removal of Impacted Mandibular Third Molars (A-PRF+: Advanced Platelet Rich Fibrin)
NCT05824793
The Use of Injectable-Platelet Rich Fibrin (i-PRF) in the Lower Third Molar Extraction
NCT06073535
Third Molars Extraction and Periodontal Disease
NCT06520137
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
PARALLEL
TREATMENT
QUADRUPLE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Test group
Application of EMD after the extraction
Application of Enamel Matrix Derivatives
After the extraction of the impacted lower third molar, EMD will be applied on the distal site of the second molar
Extraction of the impacted third molar
Extraction of the impacted third molar
Control
No application of EMD after the extraction
Extraction of the impacted third molar
Extraction of the impacted third molar
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Application of Enamel Matrix Derivatives
After the extraction of the impacted lower third molar, EMD will be applied on the distal site of the second molar
Extraction of the impacted third molar
Extraction of the impacted third molar
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Systemically healthy patients
* Non-smokers or less than 10 cigarettes per day
Exclusion Criteria
* Medication that potentially affects bone metabolism
* Absence of adjacent lower second molar
* Presence of crowns, distal caries or distal fillings of the adjacent second molar
18 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Universidad Complutense de Madrid
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
23/308-EC_X
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.