Comparison Between Single Implant Retained Partial Over-denture and Conventional Partial Denture
NCT ID: NCT03324789
Last Updated: 2017-10-30
Study Results
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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UNKNOWN
NA
18 participants
INTERVENTIONAL
2017-12-31
2018-12-31
Brief Summary
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Detailed Description
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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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Keywords
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
SINGLE
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.
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.
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 .
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 .
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.
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 .
Eligibility Criteria
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Inclusion Criteria
* 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
* 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
ALL
Yes
Sponsors
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Cairo University
OTHER
Responsible Party
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Radwa Ahmed Abdel Wanis
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
Countries
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Central Contacts
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Facility Contacts
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Sheta
Role: primary
Other Identifiers
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9999
Identifier Type: -
Identifier Source: org_study_id