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Clinical Trials/NCT06789627
NCT06789627CompletedNot Applicable

Indirect CAD/CAM Removable Partial Denture Frameworks: a Comparative Study

Cairo University1 site in 1 country30 target enrollmentStarted: October 10, 2021Last updated:
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Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
30
Locations
1
Primary Endpoint
Oral Health Related Quality of Life (OHRQoL)
Study OverviewStudy DesignEligibility CriteriaArms & InterventionsOutcomesInvestigatorsSitesRecords & IdentifiersSimilar Trials

Study Overview

Brief Summary

The aim of this study was to compare CAD Poly ether ether ketone (PEEK) RPD to CAD metallic RPD in treating partial edentulism in terms of Oral health related quality of life

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Single (Outcomes Assessor)

Eligibility Criteria

Ages
20 Years to 50 Years (Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Patients with bilateral free end saddles in the mandible (Kennedy class I) with the last standing abutment second premolar
  • •Opposing dentition is fully intact or restored to be intact
  • •Adequate inter-arch space of at least 7mm
  • •Angle's class I maxilla-mandibular relationship
  • •Patients with no periodontal disease and good oral hygiene
  • •Cooperative patients showing motivation to follow-up

Exclusion Criteria

  • •Periodontal affection of the abutment teeth
  • •Skeletal mal-relationship
  • •Unmotivated patients to maintain adequate oral hygiene and to follow up---- ---- Patients with neuro-mascular disorders
  • •Systemic disease affecting periodontal health like uncontrolled diabetes

Arms & Interventions

RPD with metallic framework

Active Comparator

Indirectly CAD/CAM produced Metallic framework

Intervention: RPD with metallic framework (Other)

RPD with PEEK framework

Experimental

Indirectly CAD/CAM produced PEEK framework

Intervention: RPD with PEEK framework (Other)

Outcomes

Primary Outcomes

Oral Health Related Quality of Life (OHRQoL)

Time Frame: 2 years

measured by Oral Health Impact Profile- 14 Minimum score 0 , Maximum score 56 higher scores indicate worse OHRQoL

Secondary Outcomes

  • Cost effectiveness(1 year)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Hend Mahmoud Mohamed Hegazi

Prinicipal investigator

Cairo University

Study Sites (1)

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