Pneumatic Sleeves and Congestive Heart Failure

Congestive Heart Failure Clinical Trial

— Sleeves-Bickel  

Official title:

The Impact of Intermittent Sequential Pneumatic Compression (ISPC) Leg Sleeves on Cardiac Performance in Patients With Congestive Heart Failure

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01691417
• Other study ID #: Sleeves-Bickel
• Status: Completed
• Phase: N/A
• First received: September 9, 2012
• Last updated: September 19, 2012

Study information

• Verified date: September 2012
• Source: Western Galilee Hospital-Nahariya
• Contact: n/a
• Is FDA regulated: No
• Health authority: Israel: Ministry of Health
• Study type: Interventional

Clinical Trial Summary

Based on the reversal of the adverse cardiovascular parameters during Laproscopic Surgery and its influence on cardiac activity in healthy subjects, the investigators expect to improved cardiac function in patients suffering from congestive heart failure.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 0
• Accepts healthy volunteers: No
• Gender: Both
• Age group: N/A and older

Eligibility

Inclusion Criteria:

• CHF (as clinically evaluated and asessed by TTE)

• Gave informed consent

• NYHA Class II-III

• LVEF equal or less than 40%

Exclusion Criteria:

• Patients who could not sign informed consent

• NYHA Class IV

• Oxygen saturation less than 90% under room air

Study Design

N/A

Related Conditions & MeSH terms

• Congestive Heart Failure
• Heart Failure

Intervention

Device:
• Intermittent Sequntial Pnumatic Compression Leg Sleeves

Locations

Country	Name	City	State
Israel	Western Galilee Hospital	Nahariya

Sponsors (1)

Lead Sponsor	Collaborator
Western Galilee Hospital-Nahariya

Country where clinical trial is conducted

Israel, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Stroke volume
Primary	Cardiac Output
Secondary	Systemic vascular resistance