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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02165072
Other study ID # L14-052
Secondary ID
Status Completed
Phase N/A
First received June 13, 2014
Last updated June 21, 2016
Start date February 2014
Est. completion date October 2015

Study information

Verified date June 2016
Source Texas Tech University Health Sciences Center
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Observational

Clinical Trial Summary

This is an observational study that will examine the possibility of determining the type of Acute Kidney Injury (AKI) using bedside ultrasound machines.


Description:

The investigators hypothesize that different types of AKI (pre-renal, renal, and post-renal) are associated with different inferior vena cava diameters and collapsibility index. The investigators will include subjects ages 18-89 years with AKI (creatinine of 2mg/100ml or higher for less than 24 hours from baseline creatinine ≤1.2 or with unknown baseline creatinine). Standard of care treatment will not be different for patients taking part in this study. Participants will have bedside ultrasounds on days 0, 1, and 3, and baseline and follow-up data will be collected from medical records.


Recruitment information / eligibility

Status Completed
Enrollment 30
Est. completion date October 2015
Est. primary completion date October 2015
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 89 Years
Eligibility Inclusion Criteria:

1. Creatinine of 1.7 mg/100ml or higher for less than 24 hours from baseline creatinine =1.2 or with unknown baseline creatinine

2. Age range: 18-89 years

3. Age range = 18

Exclusion Criteria:

1. Only chronic renal disease will exclude a patient from our study regardless of past medical history and medications they are taking. (For the purposes of this study, any patient with creatinine higher than 1.2 mg /100ml for more than 24 hours will be identified as having chronic renal disease.)

Study Design

Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
United States Texas Tech Univrsity Health Science Center Lubbock Texas

Sponsors (1)

Lead Sponsor Collaborator
Texas Tech University Health Sciences Center

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Maximum and Minimum Diameters of the Inferior Vena Cava in Patients With Acute Kidney Injury The investigators will measure the maximum and minimum diameters of the inferior vena cava with patients with acute kidney injury. Day 1 of ICU admission No
Primary Percent Collapse of the Inferior Vena Cava in Patients With Acute Kidney Injury The investigators will measure the maximum and minimum diameters of the inferior vena cava with patients with acute kidney injury and calculate the percent change between the maximum and minimum diameters. Day 1 of ICU admission No
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