CompletedNot Applicable

LifeFlow Fluid Study- Non- Critical Pediatric Patients Having a Trans Abdominal Ultrasound

United States30 participantsStarted 2018-10-02

Plain-language summary

This is an unblinded, randomized control study examining two fluid delivery modalities for non-critical female patients with a planned transabdominal pelvic ultrasound requiring intravenous fluid boluses.

Who can participate

Age range1 Month – 18 Years

SexFEMALE

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Female patients older than 1 month and less than 18 years * Patients require IV crystalloid bolus fluids before a pelvic ultrasound Exclusion Criteria: * Known cardiac insufficiency or significant cardiac surgery * Hepatic insufficiency * Renal insufficiency * Any known fluid overload states (ascites, pulmonary edema) * On any diuretic or antihypertensive therapy * Known pregnancy

What they're measuring

Duration- Ultrasound Ordered to Completed

Timeframe: From ED (Emergency Department) arrival to discharge/admission, less than 12 hours

Trial details

NCT IDNCT03712189

SponsorChildren's Hospital Los Angeles

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2019-05-31

Results submitted2021-01-25

View on ClinicalTrials.gov More Dehydration in Children trials