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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT03184025
Other study ID # 2014/239
Secondary ID
Status Active, not recruiting
Phase N/A
First received June 7, 2017
Last updated June 9, 2017
Start date July 1, 2014
Est. completion date December 29, 2020

Study information

Verified date June 2017
Source Kocaeli University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim was to evaluate the clinical performance of HEMA-containing and HEMA-free all-in-one self-etch adhesives with and without a surface sealing process with a nanohybrid composite in occlusal caries restorations. The hypothesis is that the HEMA-containing and HEMA-free all-in-one self-etch adhesive and the surface sealing process would significantly effect clinical performance of occlusal restorations.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 40
Est. completion date December 29, 2020
Est. primary completion date December 29, 2014
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 55 Years
Eligibility Inclusion Criteria:

- patients who received four direct Class I composite restorations, those with good oral hygiene with no active periodontal or pulpal diseases, whose permanent first or second molar required restorations for occlusal carious lesions with neighboring teeth and were in occlusion with antagonist teeth, and were willing to return for follow-up examinations as outlined by the investigators.

Exclusion Criteria:

- patients with uncontrolled parafunction, those presenting with poor oral hygiene and disinterested in or refused oral hygiene instructions, molars and premolars with carious lesions on a surface other than the occlusal surface and in continuity with the occlusal cavity, pulp exposure during caries removal procedure or cavities with the risk of pulp exposure, having spontaneous pain or sensitivity to percussion, and patients with periodontal or gingival disease.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
dentin adhesive
HEMA-containing and HEMA-free Self-Etch dentin adhesives clinical performance with or without surface sealant

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Neslihan Tekçe

Outcome

Type Measure Description Time frame Safety issue
Primary Number of failed restorations evaluated according to the modified USPSH criteria in patients with occlusal restorations. In restorations, retention rate, color match, wear or loss of anatomic form, marginal discoloration, caries, marginal adaptation, and surface texture were scored success or failure according to modified United States Public Health Service (USPHS) criteria. According to this criteria, success restorations received Alfa (A) or Bravo (B) scores. Alfa (A) represents the ideal clinical situation; Bravo (B) is the clinically acceptable. Failed restorations received Charlie (C) or Delta (D) scores. Charlie (C) is the clinically unacceptable situations where the restorations had to be replaced; Delta (D) is the situation where the restoration is fractured, mobile or missing and needed to be replaced immediately. an average of 1 year
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