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Vit D Receptor Gene Polymorphism (VITAMIN D GENE)

A

Ajman University

Status

Completed

Conditions

Vitamin D Status

Treatments

Other: questionnaire

Study type

Observational

Funder types

Other

Identifiers

NCT05931705
(NU/CEC/2020/0339).

Details and patient eligibility

About

The present cross-sectional observational study was conducted after the university ethical committee approved the research (NU/CEC/2020/0339). This study included 376 adults in the age group of 18-40Yrs. The patient information sheet briefed the study details and usage of salivary samples. Informed consent was obtained from participants. Healthy individuals free of associated systemic conditions, individuals not under any nutritional supplementation were included in the study, and lactating mothers, smokers, and menopausal women were excluded

Full description

The present cross-sectional observational study was conducted after the university ethical committee approved the research (NU/CEC/2020/0339). This study included 376 adults in the age group of 18-40Yrs. The patient information sheet briefed the study details and usage of salivary samples. Informed consent was obtained from participants. Healthy individuals free of associated systemic conditions, individuals not under any nutritional supplementation were included in the study, and lactating mothers, smokers, and menopausal women were excluded.

Further, the subjects were divided into active and caries-free based on caries experience. Two indexing methods were utilized to record the decay status, i.e., Decay, Missing, filled (DMFT) and Pulpal, Ulcerative, Fistula (PUFA) scores. Caries active group was further divided into a High-risk group (DMFT=< 10), Moderate risk (DMFT= 4-9), and Low risk (DMFT=1-3).

Questionnaire: Baseline information was gathered, including specifics on age, sex, height, weight, dietary preferences (non-veg/veg), and dental hygiene practices.

Enrollment

376 patients

Sex

All

Ages

18 to 60 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Healthy individuals free of associated systemic conditions
  • Individuals not under any nutritional supplementation

Exclusion criteria

  • lactating mothers
  • smokers
  • menopausal women

Trial design

376 participants in 1 patient group

High risk
Treatment:
Other: questionnaire

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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