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Sponsored by: |
Redwood Regional Medical Group |
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Information provided by: | Redwood Regional Medical Group |
ClinicalTrials.gov Identifier: | NCT00463892 |
The study is designed to see if a high-resolution MRI scan of lymph node areas near where a melanoma has been removed from the skin can pick up the spread of melanoma to those lymph nodes with a high degree of accuracy.
Condition | Intervention | Phase |
---|---|---|
Melanoma |
Procedure: High-resolution contrast-enhanced MRI scan |
Phase II |
Study Type: | Interventional |
Study Design: | Diagnostic, Non-Randomized, Open Label, Uncontrolled, Parallel Assignment, Efficacy Study |
Official Title: | A Phase II Study of High-Resolution Contrast-Enhanced MRI of Regional Lymph Nodes in Patients With Clinically Localized Invasive Melanoma |
Estimated Enrollment: | 200 |
Study Start Date: | June 2007 |
Estimated Study Completion Date: | June 2013 |
Estimated Primary Completion Date: | June 2013 (Final data collection date for primary outcome measure) |
When a melanoma of the skin is diagnosed, there is some chance it can spread to nearby lymph nodes, and from there to other parts of the body. Currently, patients with melanoma at low risk for spreading to lymph nodes do not get the lymph nodes assessed except by a physical exam. Those at high risk for spreading to lymph nodes get one or more lymph nodes removed surgically to check for melanoma spread. But physical exam alone will often miss small areas of melanoma in lymph nodes; removal of lymph nodes by surgery is painful and can cause complications. Neither assessment tool is optimal.
This study is designed to see if use of very high-resolution contrast-enhanced MRI scans of lymph node areas near the primary melanoma site in the skin can accurately detect small areas of melanoma spread to those lymph nodes. If this turns out to be the case, in the future, MRI scans could potentially be an alternative for assessing lymph nodes, compared to physical exams alone or surgical removal of the lymph nodes.
In this study, patients with low risk melanoma will receive very high-resolution MRI scans of nearby lymph nodes every 6 months for 5 years of follow-up. If the MRI looks abnormal, the lymph nodes will be biopsied, and results from the biopsy compared to the results from the MRI.
Patients with high risk melanoma will get a baseline MRI of the nearby lymph nodes, and then one or more lymph nodes will be removed (usually by sentinel lymph node biopsy) regardless of the MRI results. Again, results from the biopsy will be compared to the results from the MRI. MRI's will still be repeated every 6 months to assess whether lymph nodes not removed at surgery develop any changes.
We plan to enroll 200 patients on this study and by the end of the study will have a measure of the sensitivity and specificity of high-resolution MRI scans in the detection of melanoma involvement of regional lymph nodes.
Ages Eligible for Study: | 18 Years and older |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
Contact: Jacki Malin, RN | (707) 521-3802 | jmalin@rrmginc.com |
Contact: Ann Lowry, RN | (707) 521-3814 | alowry@rrmginc.com |
United States, California | |
Redwood Regional Medical Group | Recruiting |
Sebastopol, California, United States, 95472 | |
Contact: Jacki Malin, RN 707-521-3802 jmalin@rrmginc.com | |
Contact: Ann Lowry (707) 521-3814 alowry@rrmginc.com | |
Principal Investigator: Peter Brett, M.D. |
Principal Investigator: | Peter Brett, M.D. | Redwood Regional Medical Group |
Principal Investigator: | David Feinberg, M.D., Ph.D. | Redwood Regional Medical Group |
Responsible Party: | Redwood Regional Medical Group ( Peter Brett, M.D. ) |
Study ID Numbers: | RRMG #07-001 |
Study First Received: | April 19, 2007 |
Last Updated: | December 19, 2008 |
ClinicalTrials.gov Identifier: | NCT00463892 |
Health Authority: | United States: Institutional Review Board |
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