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OpenTrials
Completed

NCT Number: NCT01691417

Pneumatic Sleeves and Congestive Heart Failure

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.

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Key information

Conditions

Congestive Heart Failure Cardiovascular Diseases Heart Diseases Heart Failure

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Western Galilee Hospital

Nahariya, 22100, Israel

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Intermittent Sequntial Pnumatic Compression Leg Sleeves

Device

Primary outcomes

  1. Cardiac Output

Secondary outcomes

  1. Systemic vascular resistance

Other outcomes

  1. Stroke volume

Sponsors and collaborators

Lead sponsor

Western Galilee Hospital-Nahariya

Other Gov

Registry information

Official study title

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

Acronym: Sleeves-Bickel

Important dates

First posted
Sep 24, 2012
Registry last updated
Sep 24, 2012

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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