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Cardiovascular Assessment Before and After Limb Amputation

This study has been withdrawn prior to enrollment.
(Department difficulties)
Sponsor:
ClinicalTrials.gov Identifier:
NCT00907712
First Posted: May 22, 2009
Last Update Posted: June 23, 2015
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by:
HaEmek Medical Center, Israel
  Purpose
Vascular lower limb amputees have an increased morbidity and mortality. The aim of the study is to evaluate the hemodynamic changes after amputation and its relation to outcome.

Condition Intervention
Diagnostic Techniques, Cardiovascular Other: cardiac echo examination

Study Type: Interventional
Study Design: Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Diagnostic

Resource links provided by NLM:


Further study details as provided by HaEmek Medical Center, Israel:

Primary Outcome Measures:
  • cardiovascular assessment [ Time Frame: week ]

Secondary Outcome Measures:
  • complications [ Time Frame: month ]

Enrollment: 0
Study Start Date: May 2009
Study Completion Date: June 2010
Primary Completion Date: June 2010 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
No Intervention: cardiovascular
cardiac echo
Other: cardiac echo examination
cardiac echo examination - before and after the surgery

  Eligibility

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • all vascular or diabetic patients before leg amputation

Exclusion Criteria:

  • traumatic amputation
  • sepsis patient
  • urgent surgery
  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00907712


Locations
Israel
Haemek Medical Center
Afula, Israel
Sponsors and Collaborators
HaEmek Medical Center, Israel
  More Information
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