- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00370136
Sentinel Node With Ultrasound Contrast in Melanoma
June 17, 2008 updated by: Rigshospitalet, Denmark
Sentinel Node Diagnostics With Ultrasound Contrast in Melanoma
The purpose is to evaluate,in 20 patients, if the sentinel node(s) in melanoma can be detected by lymph contrast ultrasound. In comparing the patients will also get lymph-scintigraphy and sentinel node detection wiht blue dye.
The goal is to improve the method for detecting sentinel node(s) in melanoma.
Study Overview
Study Type
Interventional
Enrollment (Anticipated)
20
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Copenhagen, Denmark, 2100
- Copenhagen univercity hospital, Department of Radiology, section of ultrasound
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Malignant melanoma on a extremity,
- No spread of the cancer,
- Patients over 18 years old,
Exclusion Criteria:
- Pregnancy,
- Lactating,
- Severe hart disease,
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Diagnostic
- Allocation: Non-Randomized
- Interventional Model: Single Group Assignment
- Masking: Single
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Michael B Nielsen, MDSc, Department of Radiology, section ultrasound
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
August 1, 2006
Primary Completion
March 1, 2008
Study Completion
April 1, 2008
Study Registration Dates
First Submitted
August 29, 2006
First Submitted That Met QC Criteria
August 29, 2006
First Posted (Estimate)
August 30, 2006
Study Record Updates
Last Update Posted (Estimate)
June 18, 2008
Last Update Submitted That Met QC Criteria
June 17, 2008
Last Verified
June 1, 2008
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- (KF)01288200
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.