Diagnosis and Management of Inflammatory and Infectious Diseases
2 other identifiers
observational
400
1 country
1
Brief 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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
February 17, 1978
CompletedFirst Submitted
Initial submission to the registry
November 10, 2007
CompletedFirst Posted
Study publicly available on registry
November 14, 2007
CompletedApril 30, 2026
April 23, 2026
November 10, 2007
April 29, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
H&P, labs and other clinical metrics
this is a hypothesis-generating training consult protocol
initial and follow-up clinic visits
Study Arms (1)
1
Patients with a variety of infections and inflammatory diseases.
Eligibility Criteria
Individuals with an inflammatory or infectious condition are evaluated.
You may qualify if:
- Known or suspected exposure to infection, as determined by the Principal Investigator OR Presence of signs and symptoms of an infectious or inflammatory disease
- Age range: 3 years of age and older.
- 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.
- Primary physician outside the NIH
- 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
You may not qualify if:
- Pregnant.
- 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.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
National Institutes of Health Clinical Center
Bethesda, Maryland, 20892, United States
Related Links
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Mary E Wright, M.D.
National Institute of Allergy and Infectious Diseases (NIAID)
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- OTHER
- Time Perspective
- OTHER
- Sponsor Type
- NIH
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
November 10, 2007
First Posted
November 14, 2007
Study Start
February 17, 1978
Last Updated
April 30, 2026
Record last verified: 2026-04-23