- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04434014
Proper Nutrition And Its Relation To Oral Diseases In Covid -19 Era
June 15, 2020 updated by: Samah Mohamed Kamel, October University for Modern Sciences and Arts
Proper Nutrition and Its Relationship to Oral Diseases in the Era of Corona
effect of proper diet and vitamins on the oral health and the regeneration of the taste and smell in Covid 19 patients
Study Overview
Detailed Description
effect of proper diet and vitamins on the oral health ( bleeding gums, ulcers, bad breath) also the effect of proper diet on the regeneration of the taste and smell in Covid 19 patients A diet will be followed for 2 weeks then the progress will be evaluated by making another questionnaire
Study Type
Observational
Enrollment (Anticipated)
300
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Samah Kamel, A .Prof
- Phone Number: 0020201112230444
- Email: sabdelaziz@msa.eun.eg
Study Contact Backup
- Name: Lecturer Mona abdelmoteleb
- Phone Number: 0020201001530834
- Email: mmoteleb@msa.eun.eg
Study Locations
-
-
-
Giza, Egypt
- Recruiting
- October University of Modern Sciences and Arts
-
Contact:
- Samah Mohamed Kamel, A.Prof
- Phone Number: 0020201112230444
- Email: sabdelaziz@gmail.com
-
Contact:
- lecturer Mona Abdelmoteleb
- Email: mmoteleb@msa.eun.eg
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
20 years to 60 years (Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
- the participants will answer a questionnaire then a diet will be sent to the participants
- the participants will follow the sent diet for 2 weeks then another questionnaire will be sent to the participants
Description
Inclusion Criteria:
-
Exclusion Criteria:
- chronic diseases
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
males from 20 to above 65 y
will be sub divided into 4 groups according to age sub group I from 20 - 35 sub group II from 36- 45 sub group III from 46- 65 sub group IV more than 65
|
diet containing all essential vitamins
|
female from 20 to above 65 y
will be sub divided into 4 groups according to age will be sub divided into 4 groups according to age sub group I from 20 - 35 sub group II from 36- 45 sub group III from 46- 65 sub group IV more than 65
|
diet containing all essential vitamins
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
regeneration of taste
Time Frame: 2 weeks
|
counting the fungiform papillae in 1cm x 1cm area of the tongue during the infection and after being cured
|
2 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
June 8, 2020
Primary Completion (Anticipated)
June 18, 2020
Study Completion (Anticipated)
June 28, 2020
Study Registration Dates
First Submitted
June 6, 2020
First Submitted That Met QC Criteria
June 15, 2020
First Posted (Actual)
June 16, 2020
Study Record Updates
Last Update Posted (Actual)
June 16, 2020
Last Update Submitted That Met QC Criteria
June 15, 2020
Last Verified
June 1, 2020
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 12345678
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
No
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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