Satisfaction With Placement of Implantable Venous Access Devices in Patients With Solid Tumors

Not Applicable

Terminated

• Conditions: Unspecified Adult Solid Tumor, Protocol Specific

• Registration Number: NCT01098643
• Lead Sponsor: Vanderbilt University

Brief Summary

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.

Detailed Description

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.

Study Timeline

• Study Start: 2009-10
• Status Verified: 2010-03
• Study First Submitted: 2010-04-02
• Study First Submitted QC: 2010-04-02
• Study First Posted: 2010-04-05
• Primary Completion: 2011-09
• Study Completion: 2011-09
• Last Update Submitted: 2017-03-30
• Last Update Posted: 2017-04-04

Recruitment & Eligibility

• Status: TERMINATED
• Sex: All
• Target Recruitment: 88

Inclusion Criteria

Not provided

Exclusion Criteria

Not provided

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Primary Outcome Measures

Name	Time	Method
Overall satisfaction with port placement	n/a - study closed

Secondary Outcome Measures

Name	Time	Method
Frequency of complications
Frequency of port failure
Need for removal of device

Trial Locations

Locations (2)

Vanderbilt-Ingram Cancer Center; 🇺🇸 Nashville, Tennessee, United States

Vanderbilt-Ingram Cancer Center - Cool Springs; 🇺🇸 Nashville, Tennessee, United States