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Not yet recruiting NCT06949917

The Effect of Body Mass Index on Taste Perception,Salivary Hormones and Oral Health Status

— Observational Oral Health Tast Perference

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: body mass index for age.
Who it may be relevant to
Registry conditions: Oral Health, Tast Perference. Basic parameters: 16 years — 17 years · Female.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Center list to be confirmed — check the primary protocol.
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

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Official title

Taste Perception,Oral Health Status and Selectied Salivary Hormones in Relation to Body Mass Index Among Agroup of Iraqi Adolescent Girls.

Overview

the goal of the study is to test the effect of body mass index on adolesent Iraqi student girls by measuring salivary hormones (ghrelin,leptin,resistin)and measuring oral health by plague index score() and taste perception score () 90 female subject will be enrolled in this study between 16-17 years old,30 subjects with normal body weight ,30 subject overweight ,and 30 subject with obeiece group catogerize by body mass index according to age. the methed of the study is by taking Saliva sample from the subject , taste perception score and oral health measure.

Interventions

  • Dietary supplement body mass index for age
    different body mass index according to age (normal weight,overweight,obeiece)

Primary outcome measures

  • taste perception [Time frame: taste perception for 90 subject of different body mass index]
  • oral health status [Time frame: oral health status will be measured for 90 subject of different body mass index.]
Secondary outcome measures (3)
  • salivary ghrelin hormone [Time frame: Baseline :salivary collection for ghrelin , salivary leptin and salivary resistin in AL least two hours fasting for different body mass index subject]
  • salivary leptin hormone [Time frame: Baseline :salivary collection for ghrelin , salivary leptin and salivary resistin in AL least two hours fasting for different body mass index subject]
  • salivary resistin hormone [Time frame: Baseline :salivary collection for ghrelin , salivary leptin and salivary resistin in AL least two hours fasting for different body mass index subject]

Eligibility criteria

Inclusion criteria

  • female
  • 16-17 years old
  • subject with no systemic diseas.

Exclusion criteria

  • medically compressed patient
  • patient with systemic disease

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Observational model
Case-crossover

Study locations

Center list to be confirmed — check the primary protocol.

Identifiers

NCT: NCT06949917 · AL-Mustansiriyah University

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗