Ignite Creation Date:
2024-05-05 @ 9:42 AM
Last Modification Date:
2024-10-26 @ 9:02 AM
Study NCT ID:
NCT00001503
Status:
COMPLETED
Last Update Posted:
2023-06-18
First Post:
1999-11-03
Brief Title:
Follow-up Protocol for Patients With CancerAIDSSkin Disease
Sponsor:
National Cancer Institute NCI
Organization:
National Institutes of Health Clinical Center CC
Study Overview
Official Title:
Follow-up for Patients Previously Enrolled on the Center for Cancer Research Protocols
Status:
COMPLETED
Status Verified Date:
2023-06
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
This protocol is to provide follow-up medicalsurgical 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
Detailed Description:
Background
Patients enrolled on CCR clinical protocols may require long term follow-up to assess outcome eg 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 procedurestests will be based on the patients 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
Patients enrolled on CCR clinical protocols may require long term follow-up to assess outcome eg 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 procedurestests will be based on the patients 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
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None
Secondary IDs
| Secondary ID | Type | Domain | Link |
|---|---|---|---|
| 96-C-0071 | None | None | None |