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Evaluation of marginal bone level around short maxillary implants

Phase 2
Recruiting
Conditions
Condition 1: Dental implant. Condition 2: Edentuous ridge atrophy.
K00-K14Presence of tooth-root and mandibular implants
Atrophy of edentulous alveolar ridge
Registration Number
IRCT2017021025662N2
Lead Sponsor
Vice chancellor for research, Tehran University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
16
Inclusion Criteria

Edentulous area of at least one tooth missed in the posterior sextant of maxilla; which is considered to be treated with implant supported fixed prosthesis; available bone height of at least 6 mm and less than 10 mm below the maxillary sinus in the area planned for implant insertion, as observed in CBCT radiograph; available bone width of at least 6 mm in the area planned for implant insertion as observed in CBCT radiograph; sinus augmentation not planned, because of medical reasons or patient's unwillingness; and patient's willing for cooperation with the study.

Exclusion criteria:
Active periodontal disease (Probing pocket depth >=4 mm with bleeding on probing); full mouth plaque score >20% at time of implant placement; full mouth bleeding score >20% at time of implant placement; smoking >10 cigarettes/day; systemic disease or conditions which influence bone metabolism; and bruxism or clenching.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Marginal bone level changes. Timepoint: At implant placement, prosthesis delivery and 6 months later. Method of measurement: a standardized radiograph is taken For evaluation of marginal bone level, CBCT viewer software is used for assessing the radiographs. the distance between bone to implant contact and platform of each implant, at mesial and distal of implants were calculated at each intervals.
Secondary Outcome Measures
NameTimeMethod
Probing depth. Timepoint: At prosthesis delivery and 6 months later. Method of measurement: O’ Michigan, Williams marking probe.;Bleeding on probing. Timepoint: At prosthesis delivery and 6 months later. Method of measurement: Bleeding on probing with O’ Michigan, Williams marking, which may happen till 30 seconds later.;Implant survival rate. Timepoint: At prosthesis delivery and 6 months later. Method of measurement: Percentage of remained implants in oral cavity at the end of study.
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