NCT07669324

Brief Summary

Aim of The Study This study aims is to evaluate color change, dentin hypersensitivity and patient satisfaction after different bleaching techniques at different time intervals. Materials(subjects)\& Methods

  • Chemically activated bleaching kit.
  • Light activated bleaching kit. This will be a randomized single-blind clinical trial, patients attending the faculty. Thirty-two patients will be selected for the study. Oral hygiene steps will be taken at the first visit, as well as scaling and polishing of the teeth. Patients will be divided into two groups according to the bleaching technique used. Group 1: chemical bleaching, Group 2: light activated bleaching. Color change measurements: Tooth color measurements will be performed at baseline T0, immediately after bleaching treatment T1, 1-week T2 and 1-month T3 after bleaching using a spectrophotometer. The whiteness index will be also calculated to verify the perceived bleaching effect. Dentin hypersensitivity will be evaluated at baseline D0, immediately after bleaching treatment D1, 1 week (D2) and 3 month (D3) after bleaching using Visual Analogue Scale VAS numbered from 0 (no pain) to 10 (maximum extreme pain). At the end of the study (3 months) a questionnaire was given to the patients to assess their satisfaction with bleaching treatment.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
30

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Feb 2025

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

February 15, 2025

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 22, 2025

Completed
21 days until next milestone

Study Completion

Last participant's last visit for all outcomes

May 13, 2025

Completed
9 months until next milestone

First Submitted

Initial submission to the registry

February 19, 2026

Completed
4 months until next milestone

First Posted

Study publicly available on registry

June 25, 2026

Completed
Last Updated

June 25, 2026

Status Verified

January 1, 2025

Enrollment Period

2 months

First QC Date

February 19, 2026

Last Update Submit

June 20, 2026

Conditions

Keywords

chemical bleachinglight activated bleachingdentin hypersensitivitycolor change

Outcome Measures

Primary Outcomes (1)

  • color change measurement

    Tooth color measurements will be performed at baseline T0, immediately after bleaching treatment T1, 1-week T2 and 1-month T3 after bleaching using a spectrophotometer. The measured values will be recorded in the units of CIELab color space. CIE L\* parameter shows the degree of lightness, a\* is indicative of redness/greenness, and b\* indicates yellowness/blueness. Variations in L\*, a\*, and b\* axes and chromatic alteration will be performed at each period and compared to baseline using the following calculation: ΔE\* = \[(ΔL\*)2 + (Δa\*)2 + (Δb\*)2\]1/2.

    three months

Secondary Outcomes (2)

  • dentin hypersensitivity

    three months

  • Whiteness index WID

    1 month

Study Arms (2)

light-activated bleaching

EXPERIMENTAL

bleaching procedure was conducted according to the manufacturer's instructions. Retractor was set in place, the teeth were dried by air stream, the lips were lubricated with Vaseline, a cheek retractor was placed, and isolation was achieved using cotton rolls and the gingival soft tissues were isolated by protective Liquidam (Philips, Andover, MA), Labial surfaces of the teeth 11, 12, 21, 22 were then covered with whitening gel in about 1-2mm thick layer. one 20 min session was done.protective eye wear for both patient and operator was used,d, the bleaching gel was applied, and agitated, and then light activation was used for the period of the session.

Other: Light activated bleaching

Chemically activated bleaching

EXPERIMENTAL

The bleaching procedure was conducted according to the manufacturer's instructions. Retractor was set in place, the teeth were dried by air stream, the lips were lubricated with Vaseline, a cheek retractor was placed, and isolation was achieved using cotton rolls and the gingival soft tissues were isolated by protective Liquidam (Philips, Andover, MA), Labial surfaces of the teeth 11, 12, 21, 22 were then covered with whitening gel in about 1-2mm thick layer. one 20 min session was done.the bleaching gel was applied and agitated and then left on tooth surface for the period of the session

Other: Chemically activated bleaching

Interventions

bleaching procedure was conducted according to the manufacturer's instructions. Retractor was set in place, the teeth were dried by air stream, the lips were lubricated with Vaseline, a cheek retractor was placed, and isolation was achieved using cotton rolls and the gingival soft tissues were isolated by protective Liquidam (Philips, Andover, MA), Labial surfaces of the teeth 11, 12, 21, 22 were then covered with whitening gel in about 1-2mm thick layer. one 20 min session was done.protective eye wear for both patient and operator was used,d, the bleaching gel was applied, and agitated, and then light activation was used for the period of the session.

light-activated bleaching

The bleaching procedure was conducted according to the manufacturer's instructions. Retractor was set in place, the teeth were dried by air stream, the lips were lubricated with Vaseline, a cheek retractor was placed, and isolation was achieved using cotton rolls and the gingival soft tissues were isolated by protective Liquidam (Philips, Andover, MA), Labial surfaces of the teeth 11, 12, 21, 22 were then covered with whitening gel in about 1-2mm thick layer. one 20 min session was done.the bleaching gel was applied and agitated and then left on tooth surface for the period of the session

Chemically activated bleaching

Eligibility Criteria

Age18 Years - 45 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • Presence of six sound maxillary anterior teeth.
  • Patient having brown or yellowish stains.
  • Good oral health maintained by routine brushing.
  • Generalized tooth staining ranging from A2 or darker according to the value-oriented shade guide (Vita easy shade).
  • Patient is willing to sign a consent form and can attend all recall visits.

You may not qualify if:

  • Existing anterior crowns or any restorations on anterior teeth that will interfere with the bleaching process.
  • Smoker or alcoholic patient.
  • Patients suffering from active periodontal diseases and exposed roots.
  • Patient who undergone previous whitening procedure.
  • Pregnant and lactating women.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Nahda University

Banī Suwayf, Beni Suweif Governorate, 62511, Egypt

Location

MeSH Terms

Conditions

Dentin Sensitivity

Condition Hierarchy (Ancestors)

Tooth DiseasesStomatognathic Diseases

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
PARTICIPANT
Purpose
SCREENING
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
lecturer of operative dentistry

Study Record Dates

First Submitted

February 19, 2026

First Posted

June 25, 2026

Study Start

February 15, 2025

Primary Completion

April 22, 2025

Study Completion

May 13, 2025

Last Updated

June 25, 2026

Record last verified: 2025-01

Data Sharing

IPD Sharing
Will not share

Locations