Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
Healthy Volunteers
NCT07464197

Effectiveness of Dental Bleaching Using Different Designs of 3D-Printed and Conventional Customized Nightguards

Led by Universitat Internacional de Catalunya · Updated on 2026-03-16

40

Participants Needed

1

Research Sites

217 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This randomized, double-blind, split-mouth clinical trial evaluates the effectiveness of at-home dental bleaching using customized nightguards fabricated by digital (3D-printed CAD-CAM) and conventional methods, with and without reservoirs. Adult participants with good general and oral health and a baseline tooth shade of A2 or darker undergo bleaching with 10% carbamide peroxide. Outcomes include tooth color change (subjective and spectrophotometric measures), tooth sensitivity, gingival irritation, patient comfort, and patient satisfaction over time.

CONDITIONS

Official Title

Effectiveness of Dental Bleaching Using Different Designs of 3D-Printed and Conventional Customized Nightguards

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults aged 18 years or older
  • Good general and oral health
  • No current medical treatment (self-reported)
  • No need for surgical, endodontic, periodontal, or restorative dental treatment
  • At least six upper and six lower anterior teeth free of caries and restorations
  • Maxillary central incisors with baseline shade A2 or darker
  • Willingness to follow the study protocol and use the study-provided oral hygiene products/instructions
Not Eligible

You will not qualify if you...

  • Previous tooth bleaching treatment
  • Orthodontic appliances or prostheses that interfere with treatment
  • Severe intrinsic discoloration such as tetracycline staining, fluorosis, or discolored endodontically treated teeth
  • Pregnancy or lactation
  • Bruxism
  • Gingival recession, dentin exposure, visible enamel cracks, or other conditions linked to increased sensitivity
  • Use of anti-inflammatory or analgesic medication during the study period

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Clínica Universitària d'Odontologia UIC Barcelona

Sant Cugat del Vallès, BARCELONA, Spain, 08195

Actively Recruiting

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Research Team

M

MARTA VALLES, DDS, PhD

CONTACT

L

LISSETHE PEÑATE, DDS, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

FACTORIAL

Primary Purpose

TREATMENT

Number of Arms

4

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