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Frame (ferumoxytol) Order Form Please include the following (required): 1. Patient Demographics & Insurance Information 2. Clinical/Progress Notes, Labs, Tests supporting primary diagnosis (ICD10) ___ Patient
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Visit the official clinical trials website or platform where nct01336803 is listed.
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03
Review the inclusion and exclusion criteria to ensure you are eligible to participate.
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Contact the study coordinator or principal investigator to express interest in participating.
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Schedule screening visits and follow the instructions provided for each study procedure.
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Individuals who have the specific condition or disease being studied in nct01336803 may benefit from participating in this clinical trial.
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NCT01336803 is a unique identifier for a specific clinical trial registered on ClinicalTrials.gov.
The responsible party for filing NCT01336803 on ClinicalTrials.gov is typically the sponsor or principal investigator of the clinical trial.
The sponsor or principal investigator can fill out NCT01336803 by registering the clinical trial on ClinicalTrials.gov and providing all the required information.
The purpose of NCT01336803 is to provide a unique identifier for the clinical trial and facilitate transparency and access to information about the trial.
Information such as study design, interventions, outcomes, eligibility criteria, and contact information must be reported on NCT01336803.
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