Effect of Emergency Department Bedside Compression Ultrasonography on Door-to-Disposition Time in Patients Suspicious for Lower Extremity Deep Venous Thrombosis

NCT ID: NCT05682040

Last Updated: 2023-01-12

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

Clinical Phase

NA

Total Enrollment

50 participants

Study Classification

INTERVENTIONAL

Study Start Date

2017-11-01

Study Completion Date

2018-06-01

Brief Summary

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Comparing the disposition time of point of care ultrasound (POCUS) versus formal lower extremity doppler in emergency department patients.

Detailed Description

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Conditions

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Lower Extremity Deep Vein Thrombosis

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

DIAGNOSTIC

Blinding Strategy

NONE

Study Groups

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Active

Group Type OTHER

Bedside Compression Ultrasonography

Intervention Type DIAGNOSTIC_TEST

Point of Care Ultrasound (Bedside Compression Ultrasonography) vs formal lower extremity Doppler

Interventions

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Bedside Compression Ultrasonography

Point of Care Ultrasound (Bedside Compression Ultrasonography) vs formal lower extremity Doppler

Intervention Type DIAGNOSTIC_TEST

Eligibility Criteria

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Inclusion Criteria

\-

Exclusion Criteria

\-
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Henry Ford Health System

OTHER

Sponsor Role lead

Responsible Party

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Christopher Nedzlek

Staff physician emergency department

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Henry Ford Wyandotte Hospital

Wyandotte, Michigan, United States

Site Status

Countries

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United States

Other Identifiers

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11243

Identifier Type: -

Identifier Source: org_study_id

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