Comparison Between Single Implant Retained Partial Over-denture and Conventional Partial Denture

NCT ID: NCT03324789

Last Updated: 2017-10-30

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

18 participants

Study Classification

INTERVENTIONAL

Study Start Date

2017-12-31

Study Completion Date

2018-12-31

Brief Summary

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In this study we are going to evaluate patient satisfaction as well as the amount of bone loss on using single implant retained partial over-denture versus conventional partial denture for treatment of mandibular Kennedy class IV cases

Detailed Description

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All the procedures will be made in the outpatient clinic of the removable prosthodontics department, faculty of oral medicine, Cairo University except the CBCT will be performed in the Oral radiology department, faculty of oral medicine, Cairo University.

The selected patients will be informed of the nature of the research work and informed consent will be signed by each one of them. Only motivated patients who showed co-operation will participate in the study. Patients will be randomly divided into 2 groups.

Clinical examination and investigations will be carried out for the eligible patients including TMJ examination and intraoral examination for oral mucosa. Diagnostic charts will be prepared with full medical and dental history as well as radiographic records. The upper and lower study casts were mounted on a semi-adjustable articulator to evaluate the interarch space and the occlusal plane.

Abutment teeth will be evaluated regarding mobility, caries, existing restoration, over eruption, and malalignment. Pocket depth around the abutment teeth will be measured buccally, lingually, and proximally. Radiographic evaluation of all abutment teeth will be carried out to assess the amount of bone support, crestal bone height, continuity of lamina dura, periapical pathosis, crown/root ratio, and root form. Panoramic radiograph also to evaluate the bone quality and quantity in the lower anterior region.

All the patients will be motivated for meticulous oral hygiene.

In (Group I) The design of the finished partial overdenture will be as follows; two rests on principle abutments and lingual plate major connector. The trial of the metallic framework will be carried out for proper seat and fit.

Patients will receive anterior single implant in the mandibular sympheseal region.

The locator attachment will be inserted into the implant fixture, leaving the attachment base protruding at least 2 mm above the tissue surface. The partial overdenture will be filled with resin, and the patient will be guided to occlude in centric occlusion. The partial overdenture will be removed after the resin curing and adjusted accordingly to assure a comfortable fit.

In (Group2) The design of the finished removable partial denture will be as follows; double Aker clasp on mandibular second premolar and first molar, with no indirect retention and lingual plate as major connector .

Conditions

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Bone Loss in Jaw

Keywords

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Single implant Anterior edentulism partial denture

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Outcome Assessors
Blinding will only be done for the outcome assessor for patient satisfaction and the statistician

Study Groups

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Single Implant Partial Over-denture

The design will be as follows; two rests on principle abutments and lingual plate major connector, single implant in the symphyseal region.

Group Type EXPERIMENTAL

Single Implant Partial Over-denture

Intervention Type OTHER

Single Implant Retained Partial Over-denture will be as follows; two rests on principle abutments and lingual plate major connector, single implant in the symphyseal region.

Conventional Partial Denture

patients will receive conventional partial denture with double Aker clasp on mandibular second premolar and first molar, with no indirect retention and lingual plate as major connector .

Group Type ACTIVE_COMPARATOR

Conventional Partial Denture

Intervention Type OTHER

patients will receive conventional partial denture with double Aker clasp on mandibular second premolar and first molar, with no indirect retention and lingual plate as major connector .

Interventions

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Single Implant Partial Over-denture

Single Implant Retained Partial Over-denture will be as follows; two rests on principle abutments and lingual plate major connector, single implant in the symphyseal region.

Intervention Type OTHER

Conventional Partial Denture

patients will receive conventional partial denture with double Aker clasp on mandibular second premolar and first molar, with no indirect retention and lingual plate as major connector .

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Mandibular long span Kennedy class IV patients
* Patients with full set of opposing dentition
* Patients having enough implant bone height
* No apparent bony mal-relation.
* No intraoral soft or hard tissue pathosis
* No uncontrolled systemic diseases such as hypertension, diabetes and immunodeficiency.

Exclusion Criteria

* Drug or alcohol abuse
* A health condition precluding surgery
* Physical reasons that could affect follow-up
* Psychiatric problems
* Disorders to the implant area related to a history of radiation therapy to the head and neck, neoplasia, or bone augmentation to the implant site.
* Heavy smokers
Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Cairo University

OTHER

Sponsor Role lead

Responsible Party

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Radwa Ahmed Abdel Wanis

principal investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Radwa Sheta

Role: PRINCIPAL_INVESTIGATOR

Faculty of dentistry-Cairo Uni

Locations

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Faculty of dentistry-Cairo Uni

Giza, , Egypt

Site Status

Countries

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Egypt

Central Contacts

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Sheta

Role: CONTACT

Phone: +2001003866631

Email: [email protected]

Facility Contacts

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Sheta

Role: primary

Other Identifiers

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9999

Identifier Type: -

Identifier Source: org_study_id