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Sentinel Node With Ultrasound Contrast in Melanoma

This study has been completed.
Sponsor:
Information provided by:
Rigshospitalet, Denmark
ClinicalTrials.gov Identifier:
NCT00370136
First received: August 29, 2006
Last updated: June 17, 2008
Last verified: June 2008

August 29, 2006
June 17, 2008
August 2006
March 2008   (final data collection date for primary outcome measure)
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Complete list of historical versions of study NCT00370136 on ClinicalTrials.gov Archive Site
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Sentinel Node With Ultrasound Contrast in Melanoma
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.

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Interventional
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Allocation: Non-Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Single Group Assignment
Masking: Single Blind
Primary Purpose: Diagnostic
Malignant Melanoma
Drug: ultrasound contrast
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*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
20
April 2008
March 2008   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • Malignant melanoma on a extremity,
  • No spread of the cancer,
  • Patients over 18 years old,

Exclusion Criteria:

  • Pregnancy,
  • Lactating,
  • Severe hart disease,
Both
18 Years and older
No
Contact information is only displayed when the study is recruiting subjects
Denmark
 
NCT00370136
(KF)01288200
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Rigshospitalet, Denmark
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Principal Investigator: Michael B Nielsen, MDSc Department of Radiology, section ultrasound
Rigshospitalet, Denmark
June 2008

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP