About this trial
Periodontal disease , especially in its advanced stages , is one of the main cause for tooth loss .Tooth replacement options include dental implants , fixed partial denture , removable partial denture and complete dentures . Dental implants have become more common treatment for replacing missing teeth and aim to improve chewing efficiency, physical health and esthetic. Although conventional implants cannot be placed in every site due to resorption of the alveolar socket after extraction. Thus short implants can be used as an alternative . Hence, this study aims at comparing the clinical efficacy of short implants with standard length implants placed in native or augmented bone in patients with a history of periodontitis.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
Age group - 18 years and above
Presence of >2 mm keratinised tissue to allow flap management.
Systemically healthy patients
The residual vertical bone height at the implant sites ranging from 6 to 9 mm for short implant placement ; > 9 mm for standard implant placement.
Disqualifiers
Medical conditions contraindicating surgical interventions
Uncontrolled diabetes
Hemorrhagic disorders
Intravenous and oral bisphosphonate therapy.
Trial design
Parallel
Treatments tested in this trial
Dental Implant Surgery - short implant group (less than or equal to 6mm)
Procedure/SurgeryA mucoperiosteal flap will be raised in edentulous ridge. A short dental implant (experimental group) will be placed according to the standard protocol. The platform of the implant will be placed 2 to 3 mm below CEJ of adjacent teeth. The surgical wound closure will be coapted with mattress and single interrupted sutures
Dental Implant Surgery - Conventional implant group (greater than or equal to 10mm)
Procedure/SurgeryA mucoperiosteal flap will be raised in edentulous ridge. A standard length implant ( comparative group) ( ≥10mm) will be placed according to the standard protocol in the augmented/native bone . The platform of the implant will be placed 2 to 3 mm below CEJ of adjacent teeth. The surgical wound closure will be coapted with mattress and single interrupted sutures
Treatment groups
Trial outcomes
Primary outcomes
The primary outcome that will be assessed is implant survival rate.
The primary objective of this randomised controlled clinical trial will be to compare the survival rate of short implants (≤ 6 mm ) and standard-length implants (≥ 10 mm) in patients with a history of periodontitis; through clinical and radiographic analysis.
Sponsors and contacts
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This trial is not recruiting at the moment. You can still explore other options: