Pneumatic Sleeves and Congestive Heart Failure

Not Applicable

Completed

• Conditions: Congestive Heart Failure
• Interventions: Device: Intermittent Sequntial Pnumatic Compression Leg Sleeves

• Registration Number: NCT01691417
• Lead Sponsor: Western Galilee Hospital-Nahariya

Brief 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.

Detailed Description

Not available

Study Timeline

• Status Verified: 2012-09
• Study First Submitted: 2012-09-09
• Study First Submitted QC: 2012-09-19
• Last Update Submitted: 2012-09-19
• Study First Posted: 2012-09-24
• Last Update Posted: 2012-09-24

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: Not specified

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

• Study Type: INTERVENTIONAL
• Study Design: Not specified

Arm && Interventions

Group	Intervention	Description
Congestive Heart Failure Patients	Intermittent Sequntial Pnumatic Compression Leg Sleeves	-
Pneumatic Sleeves	Intermittent Sequntial Pnumatic Compression Leg Sleeves	-

Primary Outcome Measures

Name	Time	Method
Cardiac Output

Secondary Outcome Measures

Name	Time	Method
Systemic vascular resistance

Trial Locations

Locations (1)

Western Galilee Hospital; 🇮🇱 Nahariya, Israel