<?xml version="1.0" encoding="UTF-8"?>
<clinical_study rank="417">
  <!-- This xml conforms to an XML Schema at:
    http://clinicaltrials.gov/ct2/html/images/info/public.xsd
 and an XML DTD at:
    http://clinicaltrials.gov/ct2/html/images/info/public.dtd -->
  <required_header>
    <download_date>ClinicalTrials.gov processed this data on November 07, 2013</download_date>
    <link_text>Link to the current ClinicalTrials.gov record.</link_text>
    <url>http://clinicaltrials.gov/show/NCT00001295</url>
  </required_header>
  <id_info>
    <org_study_id>920094</org_study_id>
    <secondary_id>92-C-0094</secondary_id>
    <nct_id>NCT00001295</nct_id>
  </id_info>
  <brief_title>Continuing Care and Treatment for Patients With Cancer/AIDS/Skin Disease</brief_title>
  <official_title>Continuing Treatment for Children and Adults in the Center for Cancer Research</official_title>
  <sponsors>
    <lead_sponsor>
      <agency>National Cancer Institute (NCI)</agency>
      <agency_class>NIH</agency_class>
    </lead_sponsor>
  </sponsors>
  <source>National Institutes of Health Clinical Center (CC)</source>
  <oversight_info>
    <authority>United States: Federal Government</authority>
  </oversight_info>
  <brief_summary>
    <textblock>
      This protocol is to provide continuing medical/surgical/radio-therapeutic care, treatment
      and follow-up for NCI patients not currently entered on an active research protocol.  No
      investigational treatments will be administered on this protocol.
    </textblock>
  </brief_summary>
  <detailed_description>
    <textblock>
      Background:

      It may be in the interest of the CCR to continue to follow and treat certain subjects after
      they have completed their treatment and participation on a research protocol.

      Objective:

      To provide continuing treatment and medical follow-up for CCR subjects who have completed
      their treatment and participation on a research protocol and who are not currently entered
      on or eligible for another active research protocol.

      Eligibility:

      Subjects who have been previously enrolled on and received treatment according to an
      approved CCR research protocol. (clinical trial)

      It is in the best interest of the subject and the CCR for the subject to continue to receive
      standard care and follow-up at the NIH.

      Design:

      Medical/surgical/radiotherapeutic care, treatment and follow-up is provided for CCR subjects
      who have completed their treatment and participation on a research protocol and who are not
      currently entered on an active research protocol.

      No investigational treatments will be administered. This protocol is not be used as a
      platform to perform pilot studies of off-label uses for standard agents.
    </textblock>
  </detailed_description>
  <overall_status>Active, not recruiting</overall_status>
  <start_date>January 1992</start_date>
  <phase>N/A</phase>
  <study_type>Observational</study_type>
  <study_design>N/A</study_design>
  <enrollment type="Actual">2143</enrollment>
  <condition>Acquired Immunodeficiency Syndrome</condition>
  <condition>Neoplasm</condition>
  <condition>Skin Disease</condition>
  <condition>HIV Infections</condition>
  <eligibility>
    <criteria>
      <textblock>
        -  INCLUSION CRITERIA:

        Subjects of any age who have been previously enrolled and treated on an approved CCR
        research treatment protocol.

        It is in the best interests of the subject and the CCR for the subject to continue to
        receive treatment and follow-up at the NIH.

        The subject or guardian signs the informed consent and agrees to the proposed treatment
        regimen.

        EXCLUSION CRITERIA:

        Subjects who have not been previously treated on a CCR research treatment protocol.

        Subjects who are receiving an investigational therapy.
      </textblock>
    </criteria>
    <gender>Both</gender>
    <minimum_age>N/A</minimum_age>
    <maximum_age>N/A</maximum_age>
    <healthy_volunteers>No</healthy_volunteers>
  </eligibility>
  <overall_official>
    <last_name>Caryn Steakley, R.N.</last_name>
    <role>Principal Investigator</role>
    <affiliation>National Cancer Institute (NCI)</affiliation>
  </overall_official>
  <location>
    <facility>
      <name>National Institutes of Health Clinical Center, 9000 Rockville Pike</name>
      <address>
        <city>Bethesda</city>
        <state>Maryland</state>
        <zip>20892</zip>
        <country>United States</country>
      </address>
    </facility>
  </location>
  <location_countries>
    <country>United States</country>
  </location_countries>
  <link>
    <url>http://clinicalstudies.info.nih.gov/cgi/detail.cgi?B_1992-C-0094.html</url>
    <description>NIH Clinical Center Detailed Web Page</description>
  </link>
  <verification_date>November 2012</verification_date>
  <lastchanged_date>November 7, 2013</lastchanged_date>
  <firstreceived_date>November 3, 1999</firstreceived_date>
  <keyword>Standard Care</keyword>
  <keyword>Follow-Up</keyword>
  <keyword>Bridge Protocol</keyword>
  <is_fda_regulated>No</is_fda_regulated>
  <has_expanded_access>No</has_expanded_access>
  <condition_browse>
    <!-- CAUTION:  The following MeSH terms are assigned with an imperfect algorithm  -->
    <mesh_term>Acquired Immunodeficiency Syndrome</mesh_term>
    <mesh_term>HIV Infections</mesh_term>
    <mesh_term>Neoplasms</mesh_term>
    <mesh_term>Immunologic Deficiency Syndromes</mesh_term>
    <mesh_term>Skin Diseases</mesh_term>
  </condition_browse>
  <!-- Results have not yet been posted for this study                                -->
</clinical_study>