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COMPLETED
NCT07593508
NA

Diode Laser-Assisted Direct Pulp Capping Trial

Sponsor: Hue University of Medicine and Pharmacy

View on ClinicalTrials.gov

Summary

This randomized controlled clinical trial evaluates whether adjunctive 808-nm diode laser therapy after direct pulp capping reduces postoperative pain and dentin hypersensitivity compared with conventional Biodentine treatment. Sixty teeth from fifty-six participants with carious pulp exposure were randomly allocated into two treatment groups. Postoperative pain, dentin hypersensitivity, and 6-month clinical success rates were assessed.

Official title: Effect of Diode Laser Therapy Following Direct Pulp Capping on Postoperative Pain and Dentin Hypersensitivity: A Randomized Controlled Clinical Trial

Key Details

Gender

All

Age Range

10 Years - 58 Years

Study Type

INTERVENTIONAL

Enrollment

56

Start Date

2022-07-01

Completion Date

2024-08-31

Last Updated

2026-05-18

Healthy Volunteers

No

Interventions

DEVICE

Biodentine

Biodentine was used as a bioactive tricalcium silicate pulp-capping material placed directly over the exposed pulp tissue following hemostasis and cavity disinfection.

DEVICE

808-nm Diode Laser

Adjunctive diode laser irradiation was applied for hemostasis and disinfection before Biodentine placement during direct pulp capping.

Locations (1)

Department of Odonto-Stomatology, Hue University of Medicine and Pharmacy

Huế, Vietnam