Comparing the Diagnostic Accuracy of Clinical Dehydration Scales Among Small Children

NCT ID: NCT02249845

Last Updated: 2016-01-18

Study Results

Results pending

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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Recruitment Status

UNKNOWN

Total Enrollment

108 participants

Study Classification

OBSERVATIONAL

Study Start Date

2014-09-30

Study Completion Date

2016-08-31

Brief Summary

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The assessment of clinical dehydration scales diagnostic accuracy (CDS scale, WHO scale, Gorelick scale) among small children.

Detailed Description

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The eligible patient admitted to the hospital with acute diarrhea, after given written consent for participation in the study by the child's parents, will be clinically assessed. Dehydration syndromes noted by physician will be recorded in special form (in attachment). Than, the child will be weighted on a standard scale.

The next body mass evaluation will take place, when patient's clinical condition will by classified as good by the attending physician and the child will be at least 24 hours after finishing intravenous or probe rehydration therapy.

Conditions

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Dehydration

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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dehydration scales

children aged 1 - 36 months for CDS scale; 1 month - 5 years old for WHO scale and Gorelick scale

No interventions assigned to this group

Eligibility Criteria

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Inclusion Criteria

* age: 1 - 36 months for CDS scale; 1 month - 5 years old for WHO scale and Gorelick scale
* hospitalisation caused by acute diarrhea (acute diarrhea -increase in the frequency of evacuations ≥ 3 in 24 hours; with or without fever or vomiting)
* duration of symptoms under 5 days
* parents' written consent for child's participation in the study

Exclusion Criteria

* Dehydration caused by other mechanisms than acute diarrhea, for example dehydration caused by:

* acidosis
* kidney failure
* heart failure
* chronic liver disease
* respiratory failure
* condition after surgery
Minimum Eligible Age

1 Month

Maximum Eligible Age

5 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Medical University of Warsaw

OTHER

Sponsor Role lead

Responsible Party

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Piotr Dziechciarz, MD

Medical Doctor

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Anna Falszewska, MD

Role: PRINCIPAL_INVESTIGATOR

Medical University of Warsaw

Locations

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Department of Pediatrics, Medical University of Warsaw

Warsaw, , Poland

Site Status RECRUITING

Countries

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Poland

Central Contacts

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Anna Falszewska, MD

Role: CONTACT

+48224523309

Other Identifiers

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CDS

Identifier Type: -

Identifier Source: org_study_id

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