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Interventional Sonography Guided by Image Fusion

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT00781924
First Posted: October 29, 2008
Last Update Posted: August 8, 2011
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:
Rigshospitalet, Denmark
  Purpose
The purpose of this study is to register the precision of image fusion between live sonography and CT, MRI or PET/CT of liver lesions and other focal lesions in the abdomen. To test whether it will be possible to biopsy guided by image fusion.

Condition Intervention
Focal Liver Lesions Focal Lesions in the Abdomen Procedure: biopsy

Study Type: Observational
Study Design: Observational Model: Cohort
Time Perspective: Prospective
Official Title: Interventional Sonography Guided by Image Fusion

Resource links provided by NLM:


Further study details as provided by Rigshospitalet, Denmark:

Primary Outcome Measures:
  • Verification of the tumor by sonography [ Time Frame: baseline only ]

Estimated Enrollment: 60
Study Start Date: January 2008
Study Completion Date: September 2009
Primary Completion Date: March 2009 (Final data collection date for primary outcome measure)
Groups/Cohorts Assigned Interventions
biopsy Procedure: biopsy
ultrasound guided biopsy of tumors.

  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:   Probability Sample
Study Population
patients with focal liver lesions where biopsy is needed or the lesion has to be verified by sonography
Criteria

Inclusion Criteria:

  • Focal liver lesion seen on CT, MRI or PET/CT
  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): NCT00781924


Locations
Denmark
Rigshospitalet, Copenhagen University Hospital
Copenhagen, Denmark, 2100
Sponsors and Collaborators
Rigshospitalet, Denmark
  More Information

Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
Responsible Party: Caroline Ewertsen, Rigshospitalet
ClinicalTrials.gov Identifier: NCT00781924     History of Changes
Other Study ID Numbers: HD-2007-0066
First Submitted: October 28, 2008
First Posted: October 29, 2008
Last Update Posted: August 8, 2011
Last Verified: August 2009