NCT00338819

Brief Summary

Purpose: To test the hemodynamic profile generated by the MCS's ActiveCare+SFT device in ventilated patients and compare it to that of the Kendall SCD Express. Design: Comparative, prospective study. Patients are their own controls.

Trial Health

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

June 18, 2006

Completed
2 days until next milestone

First Posted

Study publicly available on registry

June 20, 2006

Completed
Last Updated

June 20, 2006

Status Verified

June 1, 2006

First QC Date

June 18, 2006

Last Update Submit

June 18, 2006

Conditions

DVT PreventionVentilated Patients

Keywords

DVT preventionHemodynamic studyIPCCECT

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Adult ventilated patient (Age \>18).
  • The patient or his guardian is able and voluntarily prepared to sign the Informed Consent Form.

You may not qualify if:

  • Known, preexisting DVT or PE.
  • Patient who is participating in another clinical trial.
  • Patient with contraindication to use of the device including patients with leg gangrene, recent skin graft or medical situations where increase venous and lymphatic return is undesirable.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Officials

  • Sorkine, Prof

    Tel-Aviv Sourasky Medical Center

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Sorkine, Prof

CONTACT

972-3-6973894sorkine@tasmc.health.gov.il

Study Design

Study Type
observational
Observational Model
DEFINED POPULATION
Time Perspective
OTHER
Sponsor Type
OTHER GOV

Study Record Dates

First Submitted

June 18, 2006

First Posted

June 20, 2006

Last Updated

June 20, 2006

Record last verified: 2006-06