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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT00557726
Other study ID # 780023
Secondary ID 78-I-0023
Status Recruiting
Phase
First received
Last updated
Start date February 17, 1978

Study information

Verified date May 10, 2024
Source National Institutes of Health Clinical Center (CC)
Contact Rosemary McConnell, R.N.
Phone (301) 761-6645
Email rosemary.mcconnell@nih.gov
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This protocol is being established to cover the evaluation of patients with inflammatory and/or infectious diseases which are not covered under previously existing protocols. The purpose of such a protocol is that frequently patients are referred to us with either diagnosed or undiagnosed illnesses which would be of interest to our teaching program or which would serve as a source of patients to subsequently be entered into established, ongoing protocol studies. Such patients will be admitted to the protocol and handled according to accepted medical practice of diagnosis and treatment.


Description:

Study Description: This protocol was established in 1978 to evaluate patients with diagnosed and undiagnosed inflammatory and/or infectious diseases that are of scientific interest. Once diagnosis is made patients are referred to relevant NIH protocols for follow-up. If an NIH protocol does not exist for the condition, participants receive the required clinical standard of care treatment through an outside provider or through this protocol if a provider with the necessary expertise cannot be found. It is a minimal risk study. Objective: To evaluate patients with possible infectious and/or inflammatory diseases in order to collect data/samples through the diagnosis of infectious and inflammatory conditions (including in terms of clinical, immunologic, and metabolic features) further characterize, and treat infectious and inflammatory conditions through the collection of clinical specimens, medical records and in-person assessments To provide a repository of information on enrolled participants to allow for hypothesis generation in future research


Recruitment information / eligibility

Status Recruiting
Enrollment 400
Est. completion date
Est. primary completion date
Accepts healthy volunteers No
Gender All
Age group 3 Years to 100 Years
Eligibility - INCLUSION CRITERIA: 1. Known or suspected exposure to infection, as determined by the Principal Investigator OR Presence of signs and symptoms of an infectious or inflammatory disease 2. Age range: 3 years of age and older. 3. NIAID/LIR investigator who has an interest in the patient s illness and is willing to serve as attending physician to supervise the patient's medical care at the NIH. 4. Primary physician outside the NIH 5. The patient or the patient's Legally Authorized Representative is capable of informed consent and signs the consent form. The consent form will be signed by parents or guardians of patients under the age of 18 EXCLUSION CRITERIA: 1. Pregnant. 2. Presence of conditions that, in the judgment of the investigator, may put the participant at undue risk or make them unsuitable for participation in the study.

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
United States National Institutes of Health Clinical Center Bethesda Maryland

Sponsors (1)

Lead Sponsor Collaborator
National Institute of Allergy and Infectious Diseases (NIAID)

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary H&P, labs and other clinical metrics this is a hypothesis-generating training consult protocol initial and follow-up clinic visits
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