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Evaluation of Patient Satisfaction and Biting Force of New Design of Extracoronal Attachment (O T Cap Unilateral Attachment) Versus Conventional Partial Denture for Treatment of Unilateral Mandibular Distal Extension Area

NCT ID: NCT02951507

Last Updated: 2016-11-01

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

42 participants

Study Classification

INTERVENTIONAL

Study Start Date

2017-01-31

Brief Summary

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Comparison of new design of extra coronal castable precision attachment (OT unilateral attachment) and conventional partial denture in patient satisfaction and biting force.

Detailed Description

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Conditions

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Patient Acceptance of Health Care

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Blinding Strategy

DOUBLE

Participants Investigators

Study Groups

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Conventional partial denture

Intervention will be O T unilateral attachment

Group Type ACTIVE_COMPARATOR

O T unilateral attachment

Intervention Type OTHER

O T unilateral attachment system

Conventional removal partial denture

Intervention will be new design of extra coronal attachment( O T unilateral attachment)

Group Type ACTIVE_COMPARATOR

New design of extracoronal attachment system

Intervention Type OTHER

O T unilateral attachment

Interventions

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O T unilateral attachment

O T unilateral attachment system

Intervention Type OTHER

New design of extracoronal attachment system

O T unilateral attachment

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* patients with unilateral mandibular distal extension area
* Normal crown/root ratio of last premolar
* co-operative patients

Exclusion Criteria

* completely edentulous patient
* few remaining teeth
* patients exposed to radiotherapy and chemotherapy
* patients with maxillary or mandibular defect
Minimum Eligible Age

30 Years

Maximum Eligible Age

60 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Cairo University

OTHER

Sponsor Role lead

Responsible Party

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Mohamed mamdouh afify

Principle investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Other Identifiers

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CEBD-CU-2016-10-232

Identifier Type: -

Identifier Source: org_study_id