Effect of Chemical and Light Bleaching Techniques on Color Change, Dentin Hypersensitivity and Patient Satisfaction
Comparative Evaluation of the Effect of Chemical and Light Activated Bleaching Techniques on Color Change, Dentin Hypersensitivity and Patient Satisfaction. (In-vivo Study)
1 other identifier
interventional
30
1 country
1
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
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Feb 2025
Shorter than P25 for not_applicable
1 active site
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
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 22, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
May 13, 2025
CompletedFirst Submitted
Initial submission to the registry
February 19, 2026
CompletedFirst Posted
Study publicly available on registry
June 25, 2026
CompletedJune 25, 2026
January 1, 2025
2 months
February 19, 2026
June 20, 2026
Conditions
Keywords
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
EXPERIMENTALbleaching 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.
Chemically activated bleaching
EXPERIMENTALThe 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
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.
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
Eligibility Criteria
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
- Nahda Universitylead
Study Sites (1)
Nahda University
Banī Suwayf, Beni Suweif Governorate, 62511, Egypt
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
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