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Comparison of Patients Undergoing Radial or Femoral Arterial Access for Percutaneous Catheterization-Nursing Aspects

The recruitment status of this study is unknown. The completion date has passed and the status has not been verified in more than two years.
Verified March 2008 by Hillel Yaffe Medical Center.
Recruitment status was:  Not yet recruiting
Sponsor:
ClinicalTrials.gov Identifier:
NCT00638586
First Posted: March 19, 2008
Last Update Posted: March 19, 2008
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:
Hillel Yaffe Medical Center
  Purpose

Transradial access is a recently developed alternative for diagnostic andf interventional cardiac catheterization. We sought to compare the differences between patients that have undergone PTCA transradial and transfemoral access from the nursing point of view:

  1. Anxiety levels
  2. Pain at access point, pain in general and level of pain during mobility
  3. Differences in feelings of embarrassement
  4. Differences in satisfaction

Condition
Femoral Artery Access Radial Artery Access

Study Type: Observational
Study Design: Observational Model: Case Control
Time Perspective: Prospective

Further study details as provided by Hillel Yaffe Medical Center:

Estimated Enrollment: 160
Study Start Date: April 2008
Groups/Cohorts
1
Femoral access
2
Radial access

  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
Sampling Method:   Non-Probability Sample
Study Population
All hospitalized patients that are candidates for undergoing PTCA.
Criteria

Inclusion Criteria:

  • All patients scheduled for PTCA without any exclusion criteria

Exclusion Criteria:

  • Dementia
  • Psychiatric patients
  • Unconscious
  • Minors
  • Patients who had PTCA in past
  • Patients who were initially scheduled for different access
  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): NCT00638586


Locations
Israel
Hillel Yaffe Medical Center
Hadera, Israel, 38100
Sponsors and Collaborators
Hillel Yaffe Medical Center
  More Information

ClinicalTrials.gov Identifier: NCT00638586     History of Changes
Other Study ID Numbers: HY/102008
First Submitted: March 12, 2008
First Posted: March 19, 2008
Last Update Posted: March 19, 2008
Last Verified: March 2008