MedPath

evaluation of ethanol wet bonding technique on sensitivity level of composite restoratio

Phase 3
Conditions
evaluation of post op sensitivity.
Registration Number
IRCT2016060228218N1
Lead Sponsor
Vice chancellor for research of Mashhad University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
24
Inclusion Criteria

The inclusion criteria:
Patients who have at least three premolars with a class 2 cavity (MO, DO) on each and they can be isolated; After elimination of carious tissue, the gingival margins of all cavities should be placed 1.0 mm above the cemento-enamel junction, 1-1.5 mm in axial depth and ½-2/3 of inter cuspal space in width; The restorative procedure can be performed without need to direct/indirect pulp treatment.
The exclusion criteria:
Patients exhibiting severe to moderate periodontitis; untreated periodontal disease; uncontrolled caries; marginal recession of the tooth; very poor oral hygiene; heavy occlusal forces such as bruxism and clenching; xerostomia; patients with removable prosthesis or orthodontics appliances or receiving bleaching treatments or ?uoride supplements.
Prior to treatment, A Visual Analogue Scale (VAS) is used to assess the patients' opinions toward sensitivity and those with moderate to severe sensitivity (Score 3=) are excluded from the study.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Post op sensititvity to cold stimuli. Timepoint: 1,3,7,14 and 30 days post op. Method of measurement: using VAS (Visual Analoge Scale).
Secondary Outcome Measures
NameTimeMethod
Post op sensititvity to cold stimuli. Timepoint: in 1,3,7,14,30 days. Method of measurement: using VAS (Visual Analoge Scale).
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