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Evaluation of hypersensitivity after composite resin restorations in posterior teeth made by undergraduate students

Evaluation of postoperatory hypersensitivity in class I and II composite resin restorations made by undergraduate students

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
REBEC
Registry ID
RBR-3wvgrz
Enrollment
Unknown
Registered
2020-03-23
Start date
2019-10-09
Completion date
Unknown
Last updated
2025-10-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Composite resin

Interventions

V03.175.500
The general purpose of this study is to evaluate the presence of postoperatory hypersensitivity in patients that will receive class I and II composite resin restorations in posterior teeth of patient
Other

Sponsors

Ana Paula Rodrigues de Magalhães-Chaves
Lead Sponsor
Universidade Paulista
Collaborator

Eligibility

Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Above 18 years-old; both genders; good general health; good oral higiene; received at least one direct composite restoration class I or class II in UNIP's clinics; at least 20 teeth in the mouth.

Exclusion criteria

Exclusion criteria: Presence of unilateral cross-bite; presence of previous dental hypersensitivity; restoration carried out was considered superficial, or, 0.5-1.0 mm bellow enamel-dentin junction; teeth with all cusps compromised; teeth without pulp vitality or with endodontic treatment; smokers; loss of vertical dimension; parafunctional habits; periodontal disease.

Design outcomes

Secondary

MeasureTime frame
To evaluate the postoperatory hypersensitivity in 24h, 1 week, 1 and 2 months through the USPHS criteria (presence or absense), from a variation in at least 5% in the measurements of restorations with different depths (mean and deep) and liner (presence or absence).

Primary

MeasureTime frame
To evaluate the postoperatory hypersensitivity in 24h, 1 week, 1 and 2 months through the USPHS criteria (presence or absense), from a variation in at least 5% in the measurements of group class I in relation to class II.

Countries

Brazil

Contacts

Public ContactAna Paula Rodrigues de Magalhães-Chaves

Ana Paula Rodrigues de Magalhães-Chaves

anapaulardm@gmail.com556232394000

Outcome results

None listed

Source: REBEC (via WHO ICTRP)