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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02764450
Other study ID # TEX-10y-2016
Secondary ID
Status Completed
Phase N/A
First received April 8, 2016
Last updated May 5, 2016
Start date April 2004

Study information

Verified date May 2016
Source BNM Clinic and Research
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This randomised, split-mouth clinical study evaluated the marginal quality of direct Class I and Class II restorations made of microhybrid composite and applied using two polymerisation protocols,


Recruitment information / eligibility

Status Completed
Enrollment 50
Est. completion date
Est. primary completion date March 2015
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 60 Years
Eligibility Inclusion Criteria:

- subjects at least 18 years old,

- require restorations due to primary caries in contralateral quadrants with opposing and adjacent tooth contact,

- having no restoration in the antagonist,

Exclusion Criteria

- allergic to resin-based materials,

- pregnant or nursing,

- periodontal disease

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Astralis 10 HPM
The cavity to be filled is in quadrant I or III
Astralis 10 RM
The cavity to be filled is in quadrant II or IV

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
BNM Clinic and Research

References & Publications (1)

Barabanti N, Gagliani M, Roulet JF, Testori T, Ozcan M, Cerutti A. Marginal quality of posterior microhybrid resin composite restorations applied using two polymerisation protocols: 5-year randomised split mouth trial. J Dent. 2013 May;41(5):436-42. doi: 10.1016/j.jdent.2013.02.009. Epub 2013 Feb 27. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Number of cavity filled with problem in marginal adaptation and in marginal discoloration Marginal quality of posterior microhybrid resin composite restorations applied using two polymerisation protocols: 5-year randomised split mouth trial.
The evaluation was done using both SQUACE and USPHS criteria
5 years
See also
  Status Clinical Trial Phase
Completed NCT00346944 - Health Effects From Removal of Amalgam Restorations in Patients With Symptoms Allegedly Related to Dental Amalgam Phase 4