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Pneumatic Sleeves and Congestive Heart Failure (Sleeves-Bickel)

W

Western Galilee Hospital-Nahariya

Status

Completed

Conditions

Congestive Heart Failure

Treatments

Device: Intermittent Sequntial Pnumatic Compression Leg Sleeves

Study type

Interventional

Funder types

Other

Identifiers

NCT01691417
Sleeves-Bickel

Details and patient eligibility

About

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.

Sex

All

Volunteers

No Healthy Volunteers

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

Trial design

0 participants in 2 patient groups

Pneumatic Sleeves
Experimental group
Treatment:
Device: Intermittent Sequntial Pnumatic Compression Leg Sleeves
Congestive Heart Failure Patients
Experimental group
Treatment:
Device: Intermittent Sequntial Pnumatic Compression Leg Sleeves

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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