Evaluation of the Effect of Flowable Composites on Postoperative Sensitivity in Class I Restorations.

Evaluation of Dental Restorations

Status

Recruiting

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT07343050

Enrollment

120

Registered

2026-01-15

Start date

2025-05-16

Completion date

2027-08-01

Last updated

2026-01-15

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

Conditions

Dentin Caries

Brief summary

The aim of this study is to evaluate the effect of flowable conventional and bulk-fill composites on postoperative sensitivity in class I cavities over long-term follow-up. The hypothesis to be tested in this study is that the type of composite material will not affect clinical success.

Interventions

OTHERDental restorations

Composite restorations

Study design

Observational model

CASE_CONTROL

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

ALL

Age

18 Years to No maximum

Healthy volunteers

Yes

Inclusion criteria

* good general health * no heart disease * no diabetes * no systemic diseases such as hypertension

Exclusion criteria

* Patients with advanced periodontitis and associated postoperative sensitivity, * Pregnant and breastfeeding women, * Patients undergoing orthodontic treatment, * Patients using appliances, * Patients with direct pulp capping

Design outcomes

Primary

Measure	Time frame	Description
FDI criteria	2 years	good, very good, poor

Countries

Turkey (Türkiye)

Contacts

Primary ContactMuhammet Karadaş

muhammetkaradas@gmail.com05383120177

Backup ContactElanur Yıldızoğlu

elanur.yildizoglu@erdogan.edu.tr05535658285

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026