TerminatedNot Applicable

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

Stopped: not enough pts for available to reach goal

United States88 participantsStarted 2009-10

Plain-language 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.

Who can participate

Age range18 Years – 120 Years

SexALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

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

What they're measuring

Overall satisfaction with port placement

Timeframe: n/a - study closed

Trial details

NCT IDNCT01098643

SponsorVanderbilt University

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2011-09

View on ClinicalTrials.gov More Unspecified Adult Solid Tumor, Protocol Specific trials