Status:
UNKNOWN
Posterior Implant-Supported Modified Monolithic Zirconia and Metal-Ceramic Single Crowns: 5 Years Study
Lead Sponsor:
Jordan University of Science and Technology
Collaborating Sponsors:
ITI International Team for Implantology, Switzerland
Conditions:
Posterior Occlusion
Fracture
Eligibility:
All Genders
21-55 years
Phase:
NA
Brief Summary
The outcome of implant therapy has been presented in the majority of clinical studies by focusing only on implant survival without providing detailed information on the reconstructions . However, for ...
Detailed Description
Background: Dental implants restored with single crowns (SCs) have been reported to have a comparable survival rate and fewer technical complications compared to multiple-unit implant-supported FDPs. ...
Eligibility Criteria
Inclusion
- · Participants will be required to sign informed consents prior to inclusion in the study.
- Aged between 21 to 55 years, with no contraindications to dental treatment.
- Need implant supported single crown in the maxillary and/or mandibular premolar and/or molar area
- No systemic disease.
- No signs of bruxism.
- Full-mouth plaque scores and full-mouth bleeding scores of \<25%
- Good overall dental health, no active caries, no active periodontal disease, and periodontal pocket depths not greater than 4 mm.
- Adequate bone height and width at areas of proposed implant sites
- Adequate interocclusal distance to accommodate the prosthesis
- Space width with mesial -distal width of at least 6 mm.
- Good oral hygiene and compliance with oral hygiene instructions as determined by the amount of plaque present on tooth surfaces
- Thick or medium gingival biotype.
- Bilateral one missing tooth being a premolar or molar in the maxilla or mandible with adjacent natural teeth.
- Fixed teeth opposing the edentulous area and a full complement of teeth or restored teeth in all other areas.
Exclusion
- Systemic disease
- Pregnant and lactating women
- Unwilling to receive radiographs
- Presence of clinically active periodontal disease as expressed by probing pocket depths 4 mm in combination with bleeding on probing
- Presence of peri-apical lesions or any other abnormalities in the region as detected on a radiograph.
- Subjects that get diagnosed with any systemic disease, start smoking, or become pregnant during the study period will be excluded from the study
Key Trial Info
Start Date :
April 2 2020
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
December 5 2024
Estimated Enrollment :
60 Patients enrolled
Trial Details
Trial ID
NCT04355325
Start Date
April 2 2020
End Date
December 5 2024
Last Update
April 22 2020
Active Locations (1)
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1
Jordan University of Science and Technology
Irbid, Jordan, 21110