Follow-up Protocol for Patients With Cancer/AIDS/Skin Disease

Breast Cancer Clinical Trial

Official title: Follow-up for Patients Previously Enrolled on the Center for Cancer Research Protocols

Status Completed

Clinical Trial Summary

This protocol is to provide follow-up medical/surgical visits for DCS patients who are long term survivors and may not currently be a participant entered on an active research protocol. No investigational treatments or standard treatments will be administered on this protocol.

Clinical Trial Description

Background:

• Patients enrolled on CCR clinical protocols may require long term follow-up to assess outcome (e.g., survival) or the effects of prior therapy.

• Keeping the primary treatment protocols open after accrual is complete in order to follow patients for long term outcome is an administrative burden on investigators and the IRB.

Objectives:

-To provide follow-up for patients who are long term survivors previously enrolled Center for Cancer Research (CCR) trial but who may not currently be enrolled on a research protocol.

Eligibility:

-Patients who were previously enrolled on a CCR protocol and who are not eligible for an active NCI intramural primary research protocol.

Design:

• The medical procedures/tests will be based on the patient's diagnosis, treatment and supporting clinical information. This is a follow-up study in which only standard tests and procedures are to be performed.

• Clinical information that is relevant to the patients prior protocols will be collected for research purposes.

• Procedures that entail more than minimal risk to the patient should not be performed for research purposes on this protocol. ;

Related Conditions & MeSH terms

• Breast Cancer
• Lymphoma
• Melanoma
• Ovarian Cancer
• Prostate Cancer

• NCT number: NCT00001503
• Study type: Observational
• Source: National Institutes of Health Clinical Center (CC)
• Status: Completed
• Start date: September 19, 1996
• Completion date: June 15, 2023