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Retention of CAD Metallic and Poly Ether Ether Ketone (PEEK) Frameworks

Retention of CAD Metallic and Poly Ether Ether Ketone (PEEK) Frameworks in Mandibular Kennedy Class I Cases: a Randomized Clinical Trial

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05670899
Enrollment
20
Registered
2023-01-04
Start date
2023-03-20
Completion date
2023-08-20
Last updated
2023-01-04

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

Conditions

Retention

Brief summary

comparing retention of CAD CAM metallic and Poly Ether Ether Ketone (PEEK) partial dentures in Kennedy class I casses

Detailed description

partially edentulous patients with Kennedy class I classification will be recruited for the trial and then randomly distributed on two groups; experimental group will receive CAD CAM PEEK partial denture and control group will receive CAD CAM metallic partial denture. then primary impressions will be made and then mouth preparation followed by secondary impression then scanning of the master cast using extra-oral scanner then designing the partial denture using blender for dental then the frame work will be printed. then frame work will be processed into either PEEK or Metal according to randomization. retention will be measured at zero and 3 months.

Interventions

PROCEDURECAD PEEK frame-work

Construction of PEEK framework will be done conventionally by lost wax technique using a vacuum press device. The wax pattern will be invested in a mold using special investment. Then it will be heated and melted to produce a mold into which PEEK will be vacuum pressed. The framework will be fitted on the master cast

Sponsors

Cairo University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
20 Years to 70 Years
Healthy volunteers
Yes

Inclusion criteria

\- Patients with bilateral free end saddles in the mandible (kennedy class I) with last standing abutment premolar. 2- Opposing dentition is fully intact or restored. 3- Sufficient inter-arch space. 4- Angle's class I maxilla-mandibular relationship.

Exclusion criteria

1. Periodontal affection of the abutment teeth. 2. Skeletal mal-relation. 3. Unmotivated patients to maintain adequate oral hygiene to follow up. 4. Patients with neuromuscular and Psychiatric disorders. 5. Systematic disease affecting bone and periodontal health. 6. Insufficient inter-arch space. 7. Patients with physical reasons that could affect follow up.

Design outcomes

Primary

MeasureTime frameDescription
retention3 monthsMeasurements are performed for each RPD at the time of denture insertion, after one month and three months later. Measurements were carried out using digital force gauge which is an advanced type of force meter device, used to measure tension or compression up to 20 Kg

Countries

Egypt

Outcome results

None listed

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