ISRCTN87835631
Completed
Not Applicable
A randomized double-blinded controlled clinical trial comparing the behaviour of one three-step etch-and-rinse (Optibond™FL), one two-step etch-and-rinse (Prime&Bond®NT™) and three self-etch adhesives systems; one two-step (Clearfil™SE Bond), one one-step/two-bottle (Xeno®III) and one one-step/one bottle (Xeno®V+) in the restoration of occlusal posterior cavities based on the FDI evaluation criteria and focusing marginal adaptation as the primary outcome.
niversity of Coimbra (Portugal)0 sites70 target enrollmentAugust 8, 2014
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- niversity of Coimbra (Portugal)
- Enrollment
- 70
- Status
- Completed
- Last Updated
- 11 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •1\. Agreement to participate in the study
- •2\. In good general and oral health
- •3\. Require class I restorations in their molar or premolar teeth due to primary carious lesions
- •4\. In permanent dentition
Exclusion Criteria
- •Patients with:
- •1\. Systemic diseases, chronic use of anti\-inflammatory, analgesic or psychotropic drugs
- •2\. Xerostomy
- •3\. Pregnancy or breastfeeding
- •4\. Periodontal surgery within the previous three months
- •5\. Orthodontic treatment within the previous three months
- •6\. Uncontrolled periodontal disease
- •7\. Bruxism
- •8\. Allergies to specific compounds
- •9\. Uncontrolled oral hygiene
Outcomes
Primary Outcomes
Not specified
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