Hydronephrosis on Ultrasound With CT Finding in Patients With Renal Colic

NCT ID: NCT01349244

Last Updated: 2014-07-09

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

COMPLETED

Total Enrollment

97 participants

Study Classification

OBSERVATIONAL

Study Start Date

2010-09-30

Study Completion Date

2012-09-30

Brief Summary

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The purpose of this study is to determine the overall sensitivity and specificity of hydronephrosis on point-of-care bedside ultrasound to identify hydronephrosis as compared to hydronephrosis found by CT.

Detailed Description

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Conditions

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Hydronephrosis Renal Colic

Study Design

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Observational Model Type

CASE_ONLY

Study Time Perspective

PROSPECTIVE

Eligibility Criteria

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Inclusion Criteria

* Emergency Department patients 18 yrs or older with suspected renal colic in whom the clinician intends to obtain a CT scan to diagnose kidney stone.
* Informed consent will be required prior to enrollment in the study.

Exclusion Criteria

* Known renal disease (any ESRD, transplant, PCKD), dementia, trauma, language barrier, incarcerated patients, and patients who do not undergo CT.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Yale University

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Christopher L Moore, MD

Role: PRINCIPAL_INVESTIGATOR

Yale University

Locations

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Yale University, Emergency Department

New Haven, Connecticut, United States

Site Status

Countries

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United States

Other Identifiers

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IRB # 1006006943

Identifier Type: -

Identifier Source: org_study_id

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