Evaluation of Chewing Efficiency of Conventional Complete Denture in Comparison to Reinforced Poly Amide Denture

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

38 participants

Study Classification

INTERVENTIONAL

Study Start Date

2018-02-01

Study Completion Date

2018-07-01

Brief Summary

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the trial is done in order to reinforce polyamide to improve its modulus of elasticity to be able to use it as a denture base material in all clinical cases

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Detailed Description

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Conditions

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Mouth, Edentulous

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Participants

Study Groups

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reinforced polyamide denture base

metal reinforced polyamide denture base

Group Type EXPERIMENTAL

polyamide

Intervention Type OTHER

metal reinforced polyamide denture base material

conventional acrylic resin denture base

conventional heat cured acrylic resin denture base

Group Type ACTIVE_COMPARATOR

heat cured acrylic resin

Intervention Type OTHER

conventional heat cured acrylic resin denture base material

Interventions

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polyamide

metal reinforced polyamide denture base material

Intervention Type OTHER

heat cured acrylic resin

conventional heat cured acrylic resin denture base material

Intervention Type OTHER

Other Intervention Names

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nylon

Eligibility Criteria

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Inclusion Criteria

1. Male or female patient with age range (45-55) completely edentulous and in good medical condition.
2. All patients have skeletal Angle's class I maxillo-mandibular relationship and have sufficient interarch distance.
3. Free from any systemic or neuromuscular disorder that might affect chewing efficiency of masticatory muscles.
4. Free from any tempro-mandibular joint disorder.
5. The patients have good oral hygiene.
6. The edentulous ridges should be covered by firm healthy mucosa.
7. Healthy and co-operative patients.

Exclusion Criteria

1. Patients with bad habits as severe clenching or bruxism, drug or alcohol addiction, moderate or heavy smoking (greater than 10 cigarettes per day).
2. Previous history of radiotherapy or chemotherapy.
3. Any skeletal problem dictates surgical intervention.
4. Patients having hormonal disorders as diabetes, thyroid or parathyroid hormonal diseases were not included.
5. Patient with xerostomia or excessive salivation.
6. No intraoral soft and hard tissue pathosis.
7. Psychiatric problems.

Minimum Eligible Age

55 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No