NCT01098643终止不适用
Patient Satisfaction With Placement of Implantable Venous Access Devices
适应症
试验速览
- 阶段
- 不适用
- 状态
- 终止
- 入组人数
- 88
- 试验地点
- 2
- 主要终点
- Overall satisfaction with port placement
研究概览
简要总结
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.
详细描述
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.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Health Services Research
入排标准
- 年龄范围
- 18 Years 至 120 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •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
排除标准
- 未提供
结局指标
主要结局
Overall satisfaction with port placement
时间窗: n/a - study closed
次要结局
- Frequency of port failure
- Need for removal of device
- Frequency of complications
研究者
Kristin Ancell
MD
Vanderbilt University
研究点 (2)
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