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Clinical Trials/NCT03777423
NCT03777423UnknownNot Applicable

Evaluation of Biting Force of Removable Partial Denture Made of Injection Molded PEEK Framework Versus Cobalt Chromium Framework in Mandibular Kennedy Class I Edentulous Cases

Cairo University1 site in 1 country30 target enrollmentStarted: January 1, 2019Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Enrollment
30
Locations
1
Primary Endpoint
Biting force

Study Overview

Brief Summary

This study is aiming to evaluate the biting force of polyetheretherketone (PEEK) framework partial dentures compared to that of cobalt-chromium ones in mandibular Kennedy class I edentulous cases hoping that polyetheretherketone (PEEK) framework removable partial dentures can improve the patient masticatory efficiency .

Study Design

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

Eligibility Criteria

Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Kennedy class 1 partially edentulous subjects indicated for framework partial denture

Exclusion Criteria

  • •Uncooperative patients
  • •Bad oral hygiene patients

Arms & Interventions

PEEK framework partial dentures

Experimental

High performance ketone polymers introduced lately.These polymer-based frameworks provide better esthetics, higher elasticity, lighter in weight, have low water sorption and solubility, and are easily repaired and reproduced.

Intervention: PEEK framework partial dentures (Device)

Cobalt-chromium framework partial dentures

Active Comparator

it is considered the gold standard framework. These frameworks are less bulky with high strength, conduct heat and electricity well, and have good durability. some disadvantages include hypersensitivity, adverse tissue reactions and bad aesthetics.

Intervention: Cobalt- chromium framework partial dentures (Device)

Outcomes

Primary Outcomes

Biting force

Time Frame: Change in baseline biting force from time of insertion, insertion after 1 month and after 3 months

Biting force of the patient wearing the removable partial denture measured by I-load sensor device.

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Amr Hatim Mohammed

Principle investigator

Cairo University

Study Sites (1)

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