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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03670394
Other study ID # Dehydration Assessment
Secondary ID
Status Completed
Phase
First received
Last updated
Start date September 10, 2018
Est. completion date April 1, 2020

Study information

Verified date April 2020
Source Oregon Health and Science University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Capillary refill is used clinically to assess multiple things in children. This is a prospective observational study of the correlation between capillary refill time and degree of dehydration in children seen in a pediatric ED.


Description:

All patient presenting to the pediatric ER at OHSU less than 10 years are eligible to be enrolled if being seen for a condition putting them at risk for dehydration including emesis, diarrhea, etc. Children will have their capillary refill time measured and then sent home with a digital scale to track their weight. This will serve as the standard for calculating percent dehydration. When a patient has reached a stable weight at 1 week we will assume this is their healthy weight. There is no intervention in the study.


Recruitment information / eligibility

Status Completed
Enrollment 178
Est. completion date April 1, 2020
Est. primary completion date April 1, 2020
Accepts healthy volunteers
Gender All
Age group 6 Months to 10 Years
Eligibility Inclusion Criteria:

- All children with chief complaint of diarrhea, emesis, nausea, abdominal pain

Exclusion Criteria:

- Any child with chronic cardiac or pulm disease, raynauds syndrome, bilateral upper extremity trauma, previously enrolled in the study, already received IVF in the previous 48hrs, surgery within 1week, osteogenesis imperfecta.

Study Design


Related Conditions & MeSH terms


Intervention

Diagnostic Test:
Capillary Refill
We are measuring capillary refill to assess it's correlation with dehydration in children

Locations

Country Name City State
United States OHSU Portland Oregon

Sponsors (1)

Lead Sponsor Collaborator
Oregon Health and Science University

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Capillary Refill time Assessing correlation of the refill time and percent dehydration 1 week
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