An observational study in Tooth Loss / Rehabilitation, sponsored by Takane Dental Clinic. Enrolling by invitation at 1 site in Japan. Open to participants aged 80 Years and older. Per ClinicalTrials.gov, last updated 2026-09-03.
Sponsored by Takane Dental Clinic · Observational
Background: In recent years, dental implants have become a popular and effective option for replacing missing teeth, even in older adults. However, there is still limited research on implant treatments in patients aged 80 and older.
Study Details: In this study, we evaluated an 80+ year-old patient who requested dental implants after tooth extraction. The treatment involved placing an implant immediately after tooth removal, combined with bone grafting materials (Bio-Oss®) and cell-based regenerative therapy (Class III regenerative medicine). The patient continues to attend routine follow-up visits.
Goal: Because dental implants can greatly improve quality of life for elderly individuals, the goal of this study is to clinically evaluate the safety and effectiveness of implant therapy combined with regenerative medicine in patients aged 80 and older.
165 studies on the registry are indexed under Tooth Loss; 44 are open to participants now.
This study's planned enrollment of 15 is below the median of 80 across 40 observational studies indexed under Tooth Loss.
Browse Tooth Loss studies →This is the only study on the registry with Takane Dental Clinic as lead sponsor.
Counted across the registry records on this site, refreshed daily.
Patients aged 80 years or older who visited the clinic/hospital requiring tooth extraction and requested dental implant therapy to restore missing teeth, and who consented to receive treatment combining Class III regenerative medicine and bone grafting materials.
Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.
Exclusion Criteria:
Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.
You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.
Informed consent
Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.
You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Implant Survival Rate
Percentage of implants that remain functional, stable, and pain-free without major complications.
Time frame: 2 year post-implantation
Eligibility is decided by the study team. Share this record with your doctor or contact the team directly.
No contact was published for this record. The registry link below has the sponsor’s details.
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