Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT00001355 · ClinicalTrials.gov registry record

Detection and Characterization of Host Defense Defects

A clinical trial of Immune Defects, sponsored by National Institute of Allergy and Infectious Diseases (NIAID).

Recruiting
Registry status
3,600
Enrollment target
1
Study location

NCT00001355: Recruiting study of Immune Defects, sponsored by National Institute of Allergy and Infectious Diseases (NIAID).

NCT00001355 is a study of Immune Defects that is actively recruiting participants, run by National Institute of Allergy and Infectious Diseases (NIAID). The registered enrollment target is 3,600 participants. The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT00001355, a study of Immune Defects, is actively recruiting participants, sponsored by National Institute of Allergy and Infectious Diseases (NIAID).

RECRUITING
Registry status
3,600 participants
Enrollment target
1
Study location

Study Summary

This protocol is designed to evaluate selected patients with documented recurrent or unusual infections and their family members for clinical and laboratory correlates of immune abnormalities. It allows long term follow up of patients with host defense defects and permits the periodic study of their blood, urine, saliva, skin, stool and vaginal specimens or wound drainage from such patients or their family members for medically indicated purposes and research studies related to understanding the genetic and biochemical bases of these diseases. This protocol may help provide patients and materials for the development of therapies for these diseases. This study will: 1. Determine the biochemical and genetic causes of inherited immune diseases affecting phagocytes (white blood cells that defend against bacterial and fungal infections) 2. Try to develop better ways to diagnose and treat patients with these diseases, and to prevent, diagnose and treat their infections Patients and family members may undergo the following procedures: * A personal and family medical history, physical examination and other procedures, which may include various blood tests; urinalysis; saliva collection; imaging studies such as chest X-ray, computed tomography (CT) or magnetic resonance imaging (MRI); and lung function studies, dental examination or eye examinations, if medically indicated. * Patients who have draining wounds will have fluid collected from these wounds for biochemical study. * Tissues removed as part of medical care, such as pieces of lung, liver, or teeth, or biopsies of these tissues will be studied. * Patients who have an immune problem that investigators wish to study further will be asked to return to NIH for follow-up visits at irregular intervals, but at least every 6 months. The visits will include an updated medical history, examination directed at the particular medical problem related to the immune disorder, follow-up of abnormal tests or treatment, and collec

Primary Outcome

The primary endpoint of this study will be determination of a discrete diagnosis of an infecting agent, an underlying susceptibility trait, or both.

Conditions Studied

Study Locations (1)

Maryland

  • National Institutes of Health Clinical Center - Bethesda

Trial Details

FieldValue
Enrollment Target 3,600 participants
Start Date 1993-09-01

What NCT00001355 shows while recruiting

NCT00001355 is an observational study that tracks outcomes without assigning an intervention. Its 3,600 participants enrollment target places it among the larger protocols in the corpus.

The record links to 1 condition, with Immune Defects appearing as the primary indexed condition, and to 0 interventions.

NCT00001355 reports a single indexed study location in Maryland.

Frequently Asked Questions

What is clinical trial NCT00001355 about?

NCT00001355 is a clinical study titled "Detection and Characterization of Host Defense Defects". This protocol is designed to evaluate selected patients with documented recurrent or unusual infections and their family members for clinical and laboratory correlates of immune abnormalities. It allows long term follow up of patients with host defense defects and permits the periodic study of their...

What is the current status of trial NCT00001355?

This trial is currently recruiting. The enrollment target is 3,600 participants. The study started on 1993-09-01.

What conditions does trial NCT00001355 study?

This clinical trial studies the following conditions: Immune Defects.

Who is sponsoring clinical trial NCT00001355?

This trial is sponsored by National Institute of Allergy and Infectious Diseases (NIAID), which has 2,006 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00001355 being conducted?

This trial has 1 study location across Maryland. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT06088498 · 3,600 participants · Phase 2

    App for Reducing Cravings to Smoke

  • NCT06501118 · 3,600 participants · NA

    Optimizing Care in Critically Ill at UCHealth by Liberalizing the Target O2 in Mechanically-ventilated ICU Patients

  • NCT06919419 · 3,600 participants · NA

    HOTSPOT Study: Implement and Evaluate the PrEP (Pre-exposure Prophylaxis) Implementation Strategy

  • NCT07091032 · 3,600 participants · NA

    Building Connections

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT00001355, the US trial registry maintained by the National Library of Medicine. NCT00001355 (large enrollment · single site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.