Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
26000 participants
OBSERVATIONAL
2005-08-31
2011-12-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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PROSPECTIVE
Study Groups
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Patients with head and neck cancer
Therapy for head and neck cancer
radiotherapy and/or drug therapy including chemotherapy, biologic therapy and targeted therapy
Interventions
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Therapy for head and neck cancer
radiotherapy and/or drug therapy including chemotherapy, biologic therapy and targeted therapy
Eligibility Criteria
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Inclusion Criteria
* Scheduled to receive radiotherapy and/or drug therapy including chemotherapy, biologic therapy and targeted therapy
* Written informed consent
Exclusion Criteria
* Patients scheduled to receive or who have received surgery are eligible for Registry participation as long as they are also scheduled to receive medical therapy.
18 Years
ALL
No
Sponsors
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Eli Lilly and Company
INDUSTRY
Responsible Party
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Principal Investigators
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Mednet Solutions
Role: STUDY_DIRECTOR
MedNet Solutions
Locations
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Mednet Solutions
Minnetonka, Minnesota, United States
Countries
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Other Identifiers
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I4E-US-S003
Identifier Type: OTHER
Identifier Source: secondary_id
13440
Identifier Type: -
Identifier Source: org_study_id
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