- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06582069
Bleaching Effect of Solo and Combined Kiwi Extract and Ozone and Their Impact on Enamel
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- A total of the 40 participants aged between (18-35 years) with no gender prediction.
- The participation will be entirely voluntary, and a signed statement of informed consent will be obtained prior to the start of the study.
- Systemically healthy subject based on medical and drug histories, a subject requiring scaling and polishing with moderate calculus with at least two non-adjacent hypersensitive teeth with Schiff scale scores >1 with air blast stimulus.
- Access to sound maxillary anterior teeth.
- Vitapan classical shades should be A3 or darker and lighter shades are not included.
Exclusion Criteria:
- Participants with poor oral hygiene.
- Participants with missing anterior teeth.
- Participants with unrealistic expectations.
- Participants with dental caries, those undergoing orthodontic treatment.
- Participants with a history of periodontal treatment, pregnant or lactating women and individuals with a history of asthma.
- Those who are allergic to kiwi or ozone skin therapy were excluded from the study.
- Smokers are excluded from the present study.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: bleaching with 2% kiwi extract.
The fresh pulpy kiwi will be bought 200 gm of kiwi fruits were cleaned, cut into round shapes and blended with 15 mL of distilled water in a blender to obtain about 50 mL of kiwi concentrate. This concentrate will be filtered and then transferred into a cooling centrifuge to be processed at 2000 rpm for about 20 minutes at a temperature of 40°C. The extract thus collected will be stored at 4°C till further use. |
Bleaching
|
|
Experimental: bleaching using 2,350 ppm ozone gas.
A 2,350 ppm ozone concentration at a 615 cc per minute flow rate will be supplied by a well-known ozone producing machine. The ppm of ozone supplied will be verified via an ozone detection device, and the ozone flow rate will be verified by a flow meter directly before the start of the experiment. Ozone gas will be distributed to the tooth surfaces through special trays to assure a perfect seal to prevent any ozone leakage and to be safely employed to humans |
Bleaching
|
|
Experimental: bleaching with 2% kiwi extract followed By 2,350 ppm ozone gas.
The fresh pulpy kiwi will be bought 200 gm of kiwi fruits were cleaned, cut into round shapes and blended with 15 mL of distilled water in a blender to obtain about 50 mL of kiwi concentrate. This concentrate will be filtered and then transferred into a cooling centrifuge to be processed at 2000 rpm for about 20 minutes at a temperature of 40°C. The extract thus collected will be stored at 4°C till further use. A 2,350 ppm ozone concentration at a 615 cc per minute flow rate will be supplied by a well-known ozone producing machine. The ppm of ozone supplied will be verified via an ozone detection device, and the ozone flow rate will be verified by a flow meter directly before the start of the experiment. Ozone gas will be distributed to the tooth surfaces through special trays to assure a perfect seal to prevent any ozone leakage and to be safely employed to humans. |
Bleaching
|
|
Experimental: bleaching with 38% hydrogen peroxide.
Application of 38% H2O2 gel for 20 minutes.
Then, the H2O2 gel will be removed, and teeth will be sprayed for 10 seconds with water from a 3-in-1 syringe
|
Bleaching
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Color change assessment
Time Frame: 24 Hours
|
all participants will be requested to return after 24 hours to permit rehydration of tooth surfaces before shade assessment Tooth Shades will then record using colorimeter.
The color change (ΔE) will be calculated using the formula: ΔE= {(ΔL) 2+ (Δa) 2+ (Δb)
|
24 Hours
|
|
Color change assessment
Time Frame: one month
|
all participants will be requested to return after one month for tooth shades recording using colorimeter.
The color change (ΔE) will be calculated using the formula: ΔE= {(ΔL) 2+ (Δa) 2+ (Δb) at one month
|
one month
|
|
Color change assessment
Time Frame: three month
|
all participants will be requested to return after one month for tooth shades recording using colorimeter.
The color change (ΔE) will be calculated using the formula: ΔE= {(ΔL) 2+ (Δa) 2+ (Δb) at three months
|
three month
|
|
Color change assessment
Time Frame: six months
|
all participants will be requested to return after one month for tooth shades recording using colorimeter.
The color change (ΔE) will be calculated using the formula: ΔE= {(ΔL) 2+ (Δa) 2+ (Δb) at six months
|
six months
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 24/3/2024
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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