Description Module
The Description Module contains narrative descriptions of the clinical trial, including a brief summary and detailed description. These descriptions provide important information about the study's purpose, methodology, and key details in language accessible to both researchers and the general public.
Description Module path is as follows:
Study -> Protocol Section -> Description Module
Description Module
Ignite Creation Date:
2026-03-26 @ 3:20 PM
Ignite Modification Date:
2026-03-26 @ 3:20 PM
NCT ID:
NCT07424820
Brief Summary:
The goal of this clinical trial is to evaluate whether the magnetic mallet technique improves primary implant stability and clinical outcomes compared with conventional drilling during dental implant placement in the posterior maxilla with soft bone quality.
The main questions it aims to answer are:
Does the magnetic mallet technique result in higher primary implant stability compared with conventional drilling?
Does the magnetic mallet technique reduce surgical trauma and related complications compared with conventional drilling?
Researchers will compare the magnetic mallet technique with conventional drilling to determine differences in implant stability, bone response, and clinical outcomes.
Participants will:
Undergo dental implant placement using either the magnetic mallet technique or conventional drilling.
Be clinically and radiographically evaluated for implant stability and postoperative outcomes during follow-up
Detailed Description:
This study is a prospective clinical trial designed to compare the magnetic mallet technique with conventional drilling for dental implant placement in the posterior maxilla characterized by soft bone quality (D4 bone). Achieving adequate primary implant stability in this region remains a clinical challenge, and techniques that preserve and condense bone may improve treatment outcomes.
The magnetic mallet technique uses controlled electromagnetic impulses to prepare the implant site through bone condensation rather than bone removal, potentially enhancing primary stability and reducing surgical trauma. In contrast, conventional drilling relies on rotational cutting instruments that remove bone and may generate heat, which can negatively affect bone vitality.
Eligible participants requiring dental implants in the posterior maxillary region will be randomly allocated to one of two groups: implant site preparation using the magnetic mallet technique or conventional drilling. All implants will be placed following standardized surgical protocols.
Primary outcomes will include the assessment of primary implant stability using objective measurement methods. Secondary outcomes will evaluate peri-implant bone response, intraoperative and postoperative complications, and overall clinical performance during follow-up.
The results of this study aim to provide clinical evidence regarding the effectiveness and safety of the magnetic mallet technique compared with conventional drilling, particularly in soft posterior maxillary bone, to support evidence-based decision-making in implant dentistry
Study:
NCT07424820
Study Brief:
Protocol Section:
NCT07424820