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Clinical Trials/CTRI/2014/07/004779
CTRI/2014/07/004779CompletedNot Applicable

Clinical Evaluation of CAD CAM fabricated Longterm provisional fixed partial dentures - A Randomised clinical trial

Saveetha university1 site in 1 country10 target enrollmentStarted: July 15, 2013Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
10
Locations
1
Primary Endpoint
clinical survival (clinical observation of fracture, cracks and decementation of fixed partial dentures), marginal adaptation , anatomical form and gingival health by modified Ryge criteria

Study Overview

Brief Summary

Provisional restorations should  provide pulp and periodontal protection, have good marginal integrity, esthetics and have sufficient durability to withstand the forces of mastication. Fracture of  provisional restoration is of concern, especially with long span fixed partial dentures, long term interim fixed  partial denture indicated for periodontally involved abutments, Bruxers, temporization of implants during healing period, complex rehabilitations.   In contrast to conventional temporary materials, the industrially produced blocks offer the advantage of high fracture resistance(Vanessa et al,2011). In addition these blocks also eliminate the problem of polymerization shrinkage which affects the fit of the restoration, good surface texture and esthetics.. Hence the purpose of the study is to compare the clinical survival , marginal fit, colour stability, and periodontal outcome of the CADCAM fabricated provisional fixed partial dentures to conventional methacrylate fixed partial dentures

Study Design

Study Type
Interventional
Allocation
Coin toss, Lottery, toss of dice, shuffling cards etc
Masking
Participant and Outcome Assessor Blinded

Eligibility Criteria

Ages
18.00 Year(s) to 65.00 Year(s) (—)
Sex
Male

Inclusion Criteria

  • •Subjects with missing teeth on either side of the mouth -subjects with abutment teeth having a bone loss 2-6mm with history of periodontal treatment -Good oral hygiene.

Exclusion Criteria

  • •subjects with poor oral hygiene compliance -Subjects with known allergic to acrylic materials.

Outcomes

Primary Outcomes

clinical survival (clinical observation of fracture, cracks and decementation of fixed partial dentures), marginal adaptation , anatomical form and gingival health by modified Ryge criteria

Time Frame: Baseline(24 hours), 1 month and 3 months

Secondary Outcomes

  • secondary caries, anatomic form, surface roughness of the provisional fixed partial dentures by modified Ryge criteria(Baseline(24 hrs), 1 month and 3 month)

Investigators

Sponsor Class
Research institution and hospital

Study Sites (1)

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