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Interventional Sonography Guided by Image Fusion

This study has been completed.
Sponsor:
Information provided by:
Rigshospitalet, Denmark
ClinicalTrials.gov Identifier:
NCT00781924
First received: October 28, 2008
Last updated: August 4, 2011
Last verified: August 2009
  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 ] [ Designated as safety issue: No ]

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

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
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
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT00781924

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

No publications provided

Responsible Party: Caroline Ewertsen, Rigshospitalet
ClinicalTrials.gov Identifier: NCT00781924     History of Changes
Other Study ID Numbers: HD-2007-0066
Study First Received: October 28, 2008
Last Updated: August 4, 2011
Health Authority: Denmark: The Regional Committee on Biomedical Research Ethics

ClinicalTrials.gov processed this record on November 25, 2014