Ignite Creation Date:
2024-05-05 @ 11:37 AM
Last Modification Date:
2024-10-26 @ 9:10 AM
Study NCT ID:
NCT00090662
Status:
RECRUITING
Last Update Posted:
2024-06-28
First Post:
2004-09-01
Brief Title:
Collection of Data and Samples From Healthy Donors for Use in Translational Research
Sponsor:
National Institute of Allergy and Infectious Diseases NIAID
Organization:
National Institutes of Health Clinical Center CC
Study Overview
Official Title:
Collection of Data and Samples From Healthy Donors for Use in Translational Research
Status:
RECRUITING
Status Verified Date:
2024-10-01
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:
Increased numbers of white blood cells called eosinophils can cause disease To investigate this disease researchers need blood urine sputum stool cerebrospinal fluid skin andor bone marrow samples to compare to samples from patients with this problem Some of the samples will be used for genetic testing or future research
This study will last for about 10 years and will include a maximum of 50 paid volunteers ages 18 to 65
This study will last for about 10 years and will include a maximum of 50 paid volunteers ages 18 to 65
Detailed Description:
This protocol is designed to provide data and samples from paid volunteers for use in translational studies of eosinophilia and parasitic diseases Donors meeting standard normal donor eligibility criteria will be recruited to undergo research procedures infrared thermography andor esophageal string test andor to donate blood body fluid andor tissue samples obtained using conventional techniques The investigational nature of the studies in which their data andor samples will be used as well as the risks and benefits of the procedures will be explained to all volunteers and a signed informed consent document will be obtained Volunteers will be compensated according to an established schedule based on the duration and discomfort of the donation Samples provided through this protocol will be used solely for in vitro research and will be assigned a unique product number The study investigators listed on this protocol will serve as the custodians of the code that links the product with a donor s identity The nature of the in vitro studies in which the data and specimens collected in this study will be used is not the subject of this protocol and will be described in general terms only since it involves several IRB-approved LPD protocols Because some of these protocols require normal controls without a history of asthma or allergic disease all subjects will undergo a standardized allergyasthma history at enrollment Serum immunoglobulin levels and a basic RAST panel may be performed on sera from some normal donors and some normal donors may be asked to undergo pulmonary function testing
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 |
|---|---|---|---|
| 04-I-0266 | None | None | None |