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Wear Assessment of Novel PEEK Telescopic Attachment for Overdenture

Wear Assessment of Novel PEEK Telescopic Attachment for Implant Retained Mandibular Overdenture

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06434142
Enrollment
20
Registered
2024-05-30
Start date
2024-02-11
Completion date
2024-05-01
Last updated
2024-05-30

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

Conditions

Attachment Disorder, Stress Disorder

Keywords

Telescopic attachment, Attachment Wear, Zirconia

Brief summary

To assess the wear of Zirconia-PEEK versus cobalt-chromium-PEEK telescopic attachments for implant retained complete mandibular overdenture. The wear of Zirconia-PEEK telescopic attachments can affect the retention of implant retained complete mandibular overdenture.

Detailed description

Twelve completely edentulous patients were randomly chosen for implant retained telescopic overdentures construction and divided into two groups, where group I was a patient with zirconia copy, and group II was with cobalt chromium CoCr copy. The PEEK was constructed for both groups as a secondary coping telescopic attachment for the denture. The wear measurements of PEEK were performed optically by using a USB digital microscope with a built-in camera connected to a compatible personal computer at different intervals of baseline, 3, 6, and 9 months. The data was statistically analyzed and compared using student t-test, ANOVA, and Post Hoc Test.

Interventions

Following the two-stage surgical protocol, two dental implant fixtures with a length of 10 mm and a diameter of 3.7 mm were inserted at the canine area of the mandibular alveolar ridge.

Sponsors

Hamada Zaki Mahross Atia
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
MALE
Age
50 Years to 70 Years
Healthy volunteers
Yes

Inclusion criteria

* completely edentulous * free from any dental or systemic diseases

Exclusion criteria

* medically ill fit patient * female patient

Design outcomes

Primary

MeasureTime frameDescription
the mean wear valuesat baselinemeasurement of the mean of wear between two test groups

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 5, 2026