- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06515561
Prevalence of Teeth Discoloration , Associated Risk Factors and the Most Common Shade Among Group of Egyptian Population
Prevalence of Teeth Discoloration and Associated Risk Factors and Determination of the Most Common Shade Among Group of Egyptian Population: Educational Hospital Based Cross Sectional Study
Study Overview
Status
Conditions
Detailed Description
Discoloration of teeth is a frequent dental finding and it is often esthetically displeasing and psychologically traumatizing to the patient (Manuel et al., 2010). Changes in the three distinct layers of the tooth; enamel, dentin and cementum are known to cause modification in the appearance of the teeth leading to a change in its light transmission and reflection properties (Watts et al., 2001). Generally, tooth discoloration is said to have occurred when there is a deviation in tooth color. Suresh and Gopi in 2010 noted that the normal color of primary teeth is bluish white, whereas the color of permanent teeth is grayish white or yellowish white. The teeth of adults usually appear more yellow or grayish yellow than those of younger persons because as one ages, the enamel becomes thinner from physiological wear, while the dentin becomes thicker from the deposition of secondary dentin. There are two types of tooth discoloration, extrinsic and intrinsic, while the extrinsic type is apparent on the outer surface of the teeth, the intrinsic type stains are coming from inside of the teeth. The main cause of intrinsic tooth discoloration is the decomposition of pulp tissue, which is the first indication of pulp death (Suresh & Gopi., 2010). Other causes of intrinsic tooth discoloration are enamel opacities, dental caries, tetracycline, minocycline and doxycycline staining, and enamel hypoplasia (Koleoso et al., 2004). These medications can leave a characteristic bright-yellow band that fluoresces under ultraviolet light (tetracycline) or a green-gray or blue-gray intrinsic staining (minocycline). Also, Fluoride can cause enamel discoloration through hypomineralization when too much of it is ingested during the early maturation stage of enamel formation. In addition, dental materials used for dental restorations like amalgam restorations, can generate corrosion products such as silver sulfide which can leave a gray-black color on the teeth.
On the other hand, extrinsic dental discoloration might be due to tea, coffee, tobacco smoking/chewing, betel nut chewing, drugs (e.g., chlorhexidine mouth rinse), iron salts, heavy metals (e.g., silver nitrate and lead), essential oils, amoxicillin-clavulinic acid, ciprofloxacin, linezolide, and glibenclamide (Kumar et al., 2012). Enamel defects, salivary dysfunction, and poor oral hygiene could be predisposing factors to extrinsic discoloration. Small pits and defects on the outer surface of the enamel can lead to an accumulation of food particles and stains from beverages, tobacco, and other topical agents on its surface causing the discoloration. Salivary dysfunction such as, decreased salivation can lead to difficulties in removing food debris from the tooth surface and can thus contribute to the staining of teeth. Conditions that are associated with a reduction in the salivation are salivary gland obstruction and infection, Sjögren syndrome, head and neck radiation therapy for cancer, chemotherapy, and multiple medications (e.g., anticholinergics, antihypertensive, antipsychotics and antihistamines). All of these can cause teeth discoloration (Patel et al., 2013).
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: sara saber, master
- Phone Number: 00201152766226
- Email: sara.saber@dentistry.cu.edu.eg
Study Contact Backup
- Name: reham nabil, ph degree
- Phone Number: 00201020249628
- Email: Reham.nabil@dentistry.cu.edu.eg
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Age 20-45 years.
- Males or females.
- Egyptians.
- Presence of at least 20 teeth in function.
- Patient compliance.
Exclusion Criteria:
- Psychologically unstable or mentally retarded participants
- Participants with severe periodontal diseases.
- Participants in need for emergency intervention
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
prevalence and severity of discoloration
Time Frame: 3 months
|
assessment of the prevalence and severity of dental discoloration among adults in the study area.
|
3 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
risk factors and their association with discoloration
Time Frame: 3 months
|
Identification of risk factors and their association with discoloration in the study population and knowing the most common teeth shade among the same group of population.
|
3 months
|
|
Most common teeth shade
Time Frame: 3 months
|
determination of most common teeth shade usingVita classical shade guide
|
3 months
|
Collaborators and Investigators
Sponsor
Investigators
- Study Director: Asmaa Yassen, ph degree, Professor at Conservative Dentistry Department, Faculty of Dentistry, Cairo University.
Publications and helpful links
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
- PREVELANCE OF DISCOLORATION
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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