Protocol for Radiofrequency Ablation of Pulmonary Neoplasms

Sponsor
Oncology Specialties, Alabama (Other)
Overall Status
Terminated
CT.gov ID
NCT00232128
Collaborator
(none)
1

Study Details

Study Description

Brief Summary

This research trial involves the development of a new treatment for lung tumors. It is for patients whose tumor cannot be surgically removed, have refused surgery, or the tumor has not responded well to other forms of treatment. This treatment uses a needle probe to deliver energy into the lung tumor. This probe is placed utilizing a CT scan image. The energy heats the tumor causing tumor cell death.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Radiofrequency Ablation of pulmonary neoplasms
N/A

Study Design

Study Type:
Interventional
Allocation:
Non-Randomized
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Protocol for Radiofrequency Ablation of Pulmonary Neoplasms
Study Start Date :
Jun 1, 2003

Outcome Measures

Primary Outcome Measures

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    19 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes

    Inclusion Criteria: The patients enrolled in this study should be judged to have sufficient survival to benefit from control of local disease and include at least one of the following:

    1. unresectable primary or metastatic lung tumors

    2. may benefit from multiple modalities of therapy

    3. chemotherapeutic or radiation oncologic options have been exhausted

    Exclusion Criteria:
    1. co-existing morbidities that preclude the use of surgery

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Comprehensive Cancer Institute Huntsville Alabama United States 35801

    Sponsors and Collaborators

    • Oncology Specialties, Alabama

    Investigators

    • Principal Investigator: Marshall T. Schreeder, M.D., Comprehensive Cancer Institute

    Study Documents (Full-Text)

    None provided.

    More Information

    Additional Information:

    Publications

    None provided.
    Responsible Party:
    , ,
    ClinicalTrials.gov Identifier:
    NCT00232128
    Other Study ID Numbers:
    • CCI LUN 02
    First Posted:
    Oct 4, 2005
    Last Update Posted:
    Jan 12, 2007
    Last Verified:
    May 1, 2006
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Jan 12, 2007