Neonatal, Infant and Toddler Salivary Study (NITS Study)
NCT ID: NCT05350982
Last Updated: 2022-04-28
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
30 participants
OBSERVATIONAL
2021-06-07
2021-08-20
Brief Summary
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Detailed Description
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Adrenal insufficiency (AI) describes the inability of the body to produce adequate levels of the vital stress hormone, cortisol. It is associated with considerable mortality and morbidity. There are numerous causes, both in adults and children. The commonest cause in children is AI secondary to steroid medication prescribed for inflammatory conditions such as arthritis and asthma. AI is usually permanent but, especially in those patients taking steroid medication, it may not be, and repeated testing may be required. Testing for AI requires measurement of cortisol. Cortisol levels change during the day (highest soon after waking) and increase in response to stress. There is a lack of data on what constitutes a normal cortisol level under different conditions in children, especially babies and very young children. The investigators would like to use salivary glucocorticoid sampling to study normal responses in children, in order to be able to better define what is abnormal, to ensure appropriate and safe management of children at risk of AI in the future. The current salivary collection techniques (SCT) require active patient participation, present a potential choking hazard, and are therefore unsuitable for very young children. The investigators have been working on a SCT suitable for neonates, infants, and toddlers. Our novel SCT uses a salivary steroid swab encased in a pacifier/dummy (SaliPac) and will enable study of normal adrenal gland function at different ages and under different conditions and disease states from which the investigators will construct normal reference ranges. The final step in the validation of the novel SCT is this patient study where usability, patient tolerability and carer acceptability will be examined.
Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Hospital Arm
Participants will be recruited to use the SalivaBio +/- SaliPac in a hospital setting. They will be provided with collecting instructions and will be guided by a member of the research team.
SalivaBio +/- SaliPac
Sterile collection swab (SalivaBio), Modified dummy (SaliPac)
Stimulated Home Arm
10 participants will be randomly selected by a random number generator. This arm will also be conducted in the Hospital, and the collection using a SalivaBio +/- SaliPac will still be observed by a member of the research team. These participants will receive the same information as those in the Hospital Arm, but will receive minimal input. This is to establish whether the collection instructions provided would be suitable to use in the home environment.
SalivaBio +/- SaliPac
Sterile collection swab (SalivaBio), Modified dummy (SaliPac)
Interventions
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SalivaBio +/- SaliPac
Sterile collection swab (SalivaBio), Modified dummy (SaliPac)
Eligibility Criteria
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Inclusion Criteria
* Patients attending the hospital for any reason but well enough to participate in the study (determined by the clinical care team)
* Siblings of patients if appropriate
* Individuals of any sex
* Aged 5 years or under
* Informed consent from parent(s)/carer(s)
Exclusion Criteria
* Mouth pathologies e.g., ulcers, infection, abscesses, injury or pain
1 Day
5 Years
ALL
Yes
Sponsors
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Sheffield Children's NHS Foundation Trust
OTHER
Responsible Party
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Locations
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Sheffield Children's NHS Foundation Trust
Sheffield, Sheffield (South Yorkshire District), United Kingdom
Countries
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References
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Tonge JJ, Keevil BG, Craig JN, Whitaker MJ, Ross RJ, Elder CJ. Salivary Steroid Collection in Children Under Conditions Replicating Home Sampling. J Clin Endocrinol Metab. 2022 Nov 23;107(11):3128-3136. doi: 10.1210/clinem/dgac419.
Other Identifiers
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SCH-2596
Identifier Type: -
Identifier Source: org_study_id
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