View Clinical Trial (Medical Research Study)
Patient Satisfaction With Placement of Implantable Venous Access Devices
| City: |
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Nashville |
| State: |
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Tennessee |
| Zip Code: |
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37232 |
| Conditions: |
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Unspecified Adult Solid Tumor, Protocol Specific |
| Purpose: |
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RATIONALE: Gathering information about patients with solid tumors who have implantable
venous access devices may help doctors learn more about patient satisfaction.
PURPOSE: This phase I trial is studying satisfaction with placement of implantable venous
access devices in patients with solid tumors.
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| Study Summary: |
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OBJECTIVES:
- To determine patient satisfaction with subcutaneous venous-access device placement in
oncology patients.
OUTLINE: Patients complete a computer-based survey while in the treatment area of the
Vanderbilt Oncology Clinic. Basic demographic information and basic information regarding
the placement of the device and complications are collected from the patient's medical
record.
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| Criteria: |
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DISEASE CHARACTERISTICS:
- Diagnosis of a solid tumor malignancy
- No hematological malignancy
- Patient at the Vanderbilt Oncology Clinic
- Has undergone placement of a subcutaneous, single-lumen venous-access device within
the past 6 months
- No patients who have had ≥ 2 venous-access devices placed by ≥ 1 department
PATIENT CHARACTERISTICS:
- Not specified
PRIOR CONCURRENT THERAPY:
- See Disease Characteristics
- Not currently undergoing preparation for or process of stem cell transplantation
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| NCT ID: |
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NCT01098643 |
| Primary Contact: |
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Principal Investigator
Kristin Ancell, MD
Vanderbilt-Ingram Cancer Center
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| Backup Contact: |
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N/A |
| Location Contact: |
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Nashville, Tennessee 37232
United States
Clinical Trials Office - Vanderbilt-Ingram Cancer Center
Phone: 800-811-8480
Site Status: Recruiting |
| Data Source: |
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ClinicalTrials.gov |
| Date Processed: |
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May 21, 2013 |
| Modifications to this listing: |
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