Possible Relation of Toll-Like Receptors and Nitric Oxide to Chronic Lung Disease
Primary Purpose
Lung Diseases
Status
Completed
Phase
Locations
United States
Study Type
Observational
Intervention
Tracheal Aspirate Fluid
Sponsored by
About this trial
This is an observational trial for Lung Diseases
Eligibility Criteria
Inclusion Criteria: Birth weight less than 1250 gm Requiring assisted ventilation Exclusion Criteria: Moribund condition Major pulmonary or cardiovascular associated anomaly
Sites / Locations
- Children's Mercy Hospital & Clinic
- Children's Hospital and Regional Medical Center (Seattle)
Outcomes
Primary Outcome Measures
Secondary Outcome Measures
Full Information
NCT ID
NCT00245167
First Posted
October 26, 2005
Last Updated
July 28, 2016
Sponsor
National Heart, Lung, and Blood Institute (NHLBI)
1. Study Identification
Unique Protocol Identification Number
NCT00245167
Brief Title
Possible Relation of Toll-Like Receptors and Nitric Oxide to Chronic Lung Disease
Official Title
TLR's, Nitric Oxide and Chronic Lung Disease: Any Connections?
Study Type
Observational
2. Study Status
Record Verification Date
March 2008
Overall Recruitment Status
Completed
Study Start Date
January 2002 (undefined)
Primary Completion Date
May 2006 (Actual)
Study Completion Date
May 2006 (Actual)
3. Sponsor/Collaborators
Name of the Sponsor
National Heart, Lung, and Blood Institute (NHLBI)
4. Oversight
5. Study Description
Brief Summary
The first objective of this study is to determine if increased expression of one or more members of the toll-like receptor (TLR) family of receptors that are found on inflammatory cells (present in the airway) precede development of chronic lung disease (CLD) of prematurity. The study will also determine if there is a significant correlation between TLRs and the severity of CLD. The second objective of this study is to determine the impact of c-administration of inhaled nitric oxide (INO) on TLR expression in infants at risk of developing CLD or with early CLD.
Detailed Description
BACKGROUND:
This study will examine the role of two members in the family of transmembrane receptors, TLRs, found on leukocytes and other cells that are upregulated in response to endotoxin and other stimuli. These substances transfer the signals that propagate inflammation and production of inflammatory cytokines. CLD of prematurity is characterized by early (first week of life) evidence of lung airway inflammation. It is unknown if TLR family members propagate this pathway.
DESIGN NARRATIVE:
This study will involve saving weekly tracheal aspirate fluid samples obtained with routine airway toilet in infants less than or equal to 1250 gm birth weight, who are admitted to a Neonatal Intensive Care unit requiring assisted ventilation via an endotracheal tube. The waste sample will be collected with the cellular contents separated by centrifugation and placed on Trizol reagent after obtaining a cell count. Later extraction and batch analysis of TLR, mRNA, and proteins as well as mRNA and protein for housekeeping genes will be performed. Immunohistochemistry will also be used to semi-quantitate the samples. Samples will be obtained in the first one to two days, and again at the end of the first week of life. In infants who were also participating in the related "Low Dose INO in CLD of Prematurity" study, in which tracheal aspirate samples were collected, when the code is broken to determine who received nitric oxide versus placebo, the second aim of the study will be carried out: to determine the impact, if any, of INO.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Lung Diseases
7. Study Design
Enrollment
120 (false)
8. Arms, Groups, and Interventions
Intervention Type
Procedure
Intervention Name(s)
Tracheal Aspirate Fluid
10. Eligibility
Sex
All
Maximum Age & Unit of Time
1 Year
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Birth weight less than 1250 gm
Requiring assisted ventilation
Exclusion Criteria:
Moribund condition
Major pulmonary or cardiovascular associated anomaly
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
William E. Troug, MD
Organizational Affiliation
Children's Mercy Hospital & Clinic
Official's Role
Principal Investigator
Facility Information:
Facility Name
Children's Mercy Hospital & Clinic
City
Kansas City
State/Province
Missouri
ZIP/Postal Code
64108
Country
United States
Facility Name
Children's Hospital and Regional Medical Center (Seattle)
City
Seattle
State/Province
Washington
ZIP/Postal Code
98195
Country
United States
12. IPD Sharing Statement
Learn more about this trial
Possible Relation of Toll-Like Receptors and Nitric Oxide to Chronic Lung Disease
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