ActiveCare+SFT Hemodynamic Profile Compare to SCD Express in Ventilated Patients

Ventilated Patients Clinical Trial

Official title:

ActiveCare+SFT Hemodynamic Profile Compare to SCD Express in Ventilated Patients

Clinical Trial Details — Status: Not yet recruiting

Administrative data

• NCT number: NCT00338819
• Other study ID #: TASMC06SP156CTIL
• Status: Not yet recruiting
• Phase: N/A
• First received: June 18, 2006
• Last updated: June 18, 2006

Study information

• Verified date: June 2006
• Source: Tel-Aviv Sourasky Medical Center
• Contact: Sorkine, Prof
• Phone: 972-3-6973894
• Email: sorkine[@]tasmc.health.gov.il
• Is FDA regulated: No
• Health authority: Israel: Israeli Health Ministry Pharmaceutical Administration
• Study type: Observational

Clinical Trial 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.

Recruitment information / eligibility

• Status: Not yet recruiting
• Enrollment: 0
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Adult ventilated patient (Age >18).

• The patient or his guardian is able and voluntarily prepared to sign the Informed Consent Form.

Exclusion Criteria:

• 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.

Study Design

Observational Model: Defined Population, Time Perspective: Cross-Sectional

Related Conditions & MeSH terms

• DVT Prevention
• Ventilated Patients

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
Tel-Aviv Sourasky Medical Center