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Four Mandibular Implant-retained Overdentures in Individuals With Type 2 Diabetes

Clinical and Radiographic Outcomes Around Four Mandibular Implant-retained Overdentures in Individuals With Type 2 Diabetes: A Long-term Retrospective Preliminary Study

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06206005
Enrollment
20
Registered
2024-01-16
Start date
2023-12-04
Completion date
2024-08-05
Last updated
2024-01-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Bone Resorption

Brief summary

Studies clinically evaluate the long-term outcome of 4 implant attachment-retained mandibular OVDs among patients with high glycemic levels are lacking.

Detailed description

Chronic hyperglycemia is considered as a typical risk-factor that causes soft tissue inflammation and bone loss around natural teeth and implants. One possible explanation for this mechanism is that chronic hyperglycemia has the propensity to increase the levels of accumulated glycation end products (AGEs) in the serum and oral tissues that accelerates the production of proinflammatory cytokines that induce bone destruction around natural teeth and implants. However, it is relevant to indicate that dental implants in chronic hyperglycemia under ideal glycemic conditions can successfully osseointegrate and show predictable outcomes over long durations in both diabetic and non-diabetic patients. Studies clinically evaluate the long-term outcome of 4 implant attachment-retained mandibular OVDs among patients with high glycemic levels are lacking.

Interventions

OTHERObservational study

evaluate implant survival, peri-implant outcome of 4 implant retained mandibular OVD after 10 years of function.

Sponsors

Menoufia University
CollaboratorOTHER
Mansoura University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
55 Years to 65 Years

Inclusion criteria

* Patients with edentulous maxilla and mandible for at least 12 months. * Patients have problems with mandibular denture retention and stability. * Patients with a mandibular bone height measured on a panoramic x-ray between 15 and 25 mm at the mandibular symphysis region.

Exclusion criteria

* Patients who did not receive implants at the department clinic. * Patients with more or less than 4 implants in the mandible. * Patients with well controlled diabetics. * Patients with relative contraindications, such as a history of parafunctional habits, daily smokers of more than 10 cigarettes, or alcoholism. * Patients who have previously received head and neck radiation therapy; furthermore, patients receiving intravenous bisphosphonates, chemotherapy, or psychological disorders could jeopardize their cooperation.

Design outcomes

Primary

MeasureTime frameDescription
Crestal bone loss around implantsThis is a retrospective study, Measurement will be performed after implants being in service by 10 yearsamount of bone loss which appears on a periapical radiograph

Secondary

MeasureTime frameDescription
Probing depthThis is a retrospective study, Measurement will be performed after implants being in service by 10 yearsBy using a plastic periodontal probe to measure the probing depth around the implants

Countries

Egypt

Contacts

Primary ContactMohammed Elsawy, PhD
Dr_sawy@windowslive.com00201061314522
Backup ContactDoaa A. mewafy, PhD
Doaamowafy@mans.edu.eg00201061133971

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026