NCT01279746

Brief Summary

The purpose of this study is to prove that bedside Ultrasound Compression is a useful screening tool for the diagnosis of occult deep vein thrombosis in patients presenting to the emergency room with hypoxia.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
100

participants targeted

Target at P50-P75 for all trials

Timeline
Completed

Started Apr 2010

Shorter than P25 for all trials

Geographic Reach
1 country

3 active sites

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

April 1, 2010

Completed
8 months until next milestone

First Submitted

Initial submission to the registry

November 23, 2010

Completed
1 month until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 1, 2011

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

January 1, 2011

Completed
18 days until next milestone

First Posted

Study publicly available on registry

January 19, 2011

Completed
Last Updated

June 23, 2015

Status Verified

June 1, 2015

Enrollment Period

9 months

First QC Date

November 23, 2010

Last Update Submit

June 21, 2015

Conditions

Hypoxia

Keywords

DVT Ultrasound compression Hypoxia Pulmonary EmboliOccult DVT in hypoxic patients

Study Arms (1)

ultrasond compression of deep veins

Device: Ultrasound compression of femoral and popliteal veins

Interventions

Ultrasound compression of femoral and popliteal veinsDEVICE

Bedside ultrasound compression of femoral and popliteal veins.

ultrasond compression of deep veins

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

patients with saturation under 94% room air

You may qualify if:

  • Patients presenting to the Emergency room
  • years or older, saturation 94% and under on room air.

You may not qualify if:

  • none

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (3)

HaEmek Medical Center

Afula, Israel, Israel

Location

HaEmek Medical Center

Afula, 13425, Israel

Location

HaEmek Medical Center

Afula, Israel

Location

MeSH Terms

Conditions

Hypoxia

Condition Hierarchy (Ancestors)

Signs and Symptoms, RespiratorySigns and SymptomsPathological Conditions, Signs and Symptoms

Study Design

Study Type
observational
Observational Model
CASE ONLY
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

November 23, 2010

First Posted

January 19, 2011

Study Start

April 1, 2010

Primary Completion

January 1, 2011

Study Completion

January 1, 2011

Last Updated

June 23, 2015

Record last verified: 2015-06

Locations

IL(3)