Azithromycin in the Prevention of Lung Injury in Premature Newborn
Primary Purpose
Bronchopulmonary Dysplasia
Status
Completed
Phase
Phase 4
Locations
Study Type
Interventional
Intervention
Azithromycin
Placebo
Sponsored by
About this trial
This is an interventional prevention trial for Bronchopulmonary Dysplasia
Eligibility Criteria
Inclusion Criteria:
- preterm infants of less than 37 weeks of gestational age who have undergone mechanical ventilation within the first 72 hours of life
Exclusion Criteria:
- Major congenital malformations or chromosomal syndromes Mothers carrying the HIV virus.
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Placebo Comparator
Arm Label
azithromycin group
placebo group
Arm Description
A control group composed of 40 newborns receiving azithromycin
comparative group composed of 40 newborns who would receive saline 0.9%
Outcomes
Primary Outcome Measures
bronchopulmonary dysplasia
neonate that needs to use oxygen in concentrations above 21% for a period greater than or equal to 28 days
Secondary Outcome Measures
TNF
decreasing in plasma levels after treatment with azitromicina
IL-10
increasing in plasma levels after treatment with azitromicina
IL-6
increasing in plasma levels after treatment with azitromicina
IL-8
increasing in plasma levels after treatment with azitromicina
IL1b
increasing in plasma levels after treatment with azitromicina
IL2
increasing in plasma levels after treatment with azitromicina
Full Information
NCT ID
NCT03485703
First Posted
March 25, 2018
Last Updated
March 25, 2018
Sponsor
Hospital de Clinicas de Porto Alegre
1. Study Identification
Unique Protocol Identification Number
NCT03485703
Brief Title
Azithromycin in the Prevention of Lung Injury in Premature Newborn
Official Title
Randomized Clinical Trial: Use of Azithromycin to Prevent Lung Damage in Preterm Newborns Under Mechanical Ventilation
Study Type
Interventional
2. Study Status
Record Verification Date
March 2018
Overall Recruitment Status
Completed
Study Start Date
August 28, 2012 (Actual)
Primary Completion Date
April 13, 2016 (Actual)
Study Completion Date
April 13, 2016 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Hospital de Clinicas de Porto Alegre
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
The introduction of invasive mechanical ventilation in the treatment of preterm infants works as an adjuvant in the treatment of acute respiratory failure, which has resulted in significantly significant survival rates. In recent years there has been an increase in the number of evidence that mechanical factors can cause lung injury through inflammatory cells and soluble mediators.
The alveolar and airway epithelium is an important source of cytokine release. Cytokines are very low molecular weight proteins or glycoproteins with hormone-like actions. They contribute to the pathogenesis of various diseases through the ability to induce other inflammatory mediators Mechanical ventilation strategies can increase pulmonary and systemic cytokines and lead to dysfunction of multiple organs and systems.
Azithromycin has a potent anti-inflammatory and immunomodulatory effect It suppresses the production of proinflammatory cytokines (IL-6, IL-1, and TNF-α), has effective antimicrobial properties against Ureaplasma and, best of all, few side effects The hypothesis of this study is that azithromycin would reduce pulmonary inflammation induced by mechanical ventilation in premature infants, conferring a protective character.Randomized clinical trial: use of azithromycin in preventing pulmonary damage newborn preterm undergoing mechanical ventilation
Detailed Description
The nature of lung injury induced by mechanical ventilation is clearly established, including the release of immunoinflammatory mediators. However, safe drug therapy that decreases its severity is not available. Azithromycin is a macrolide antibiotic with potent anti-inflammatory effects, but has been poorly studied in preterm infants except for very few studies in extreme preterms for the prevention of bronchopulmonary dysplasia.
The aim of this study was to evaluate the effect of azithromycin on the prevention of cytokine-mediated MV-induced injury in cytokine plasma levels (IL-1β, IL-2, IL-6, IL-8, IL-10 and TNF- α) in preterm newborns, submitted to mechanical ventilation in the first 72 hours of life.
It is a double-blind placebo controlled clinical trial. When the use of azithromycin was considered, after signing the informed consent, a randomization was performed by the intravenous mixtures center of Hospital de clinicas de porto alegre where a group of newborns will receive azithromycin EV at the dose of 10mg / kg / day and another group will receive placebo (SF 0.9%) in the same volume, a blood aliquot of 300μL will be collected in all ETDA for cytokine analysis and PCR for Ureaplasma. After 5 days of starting azithromycin or placebo, a new sample will be collected for cytokines along with blood collection from the patient's routine. There will be no blood collection exclusively for the study.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Bronchopulmonary Dysplasia
7. Study Design
Primary Purpose
Prevention
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Model Description
for a period of 5 days, a group of infants will receive azithromycin EV at a dose of 10 mg / kg / day and another group will receive placebo (SF 0.9%) in the same volume, every 24 hours.
Masking
None (Open Label)
Allocation
Randomized
Enrollment
80 (Actual)
8. Arms, Groups, and Interventions
Arm Title
azithromycin group
Arm Type
Experimental
Arm Description
A control group composed of 40 newborns receiving azithromycin
Arm Title
placebo group
Arm Type
Placebo Comparator
Arm Description
comparative group composed of 40 newborns who would receive saline 0.9%
Intervention Type
Drug
Intervention Name(s)
Azithromycin
Other Intervention Name(s)
group A
Intervention Description
the newborn group will receive intravenous azithromycin 10 mg / kg / day once daily for 5 days
Intervention Type
Drug
Intervention Name(s)
Placebo
Other Intervention Name(s)
group B
Intervention Description
the group of newborns will receive 0.9% saline once daily for 5 days
Primary Outcome Measure Information:
Title
bronchopulmonary dysplasia
Description
neonate that needs to use oxygen in concentrations above 21% for a period greater than or equal to 28 days
Time Frame
28 days
Secondary Outcome Measure Information:
Title
TNF
Description
decreasing in plasma levels after treatment with azitromicina
Time Frame
5 days
Title
IL-10
Description
increasing in plasma levels after treatment with azitromicina
Time Frame
5 days
Title
IL-6
Description
increasing in plasma levels after treatment with azitromicina
Time Frame
5 days
Title
IL-8
Description
increasing in plasma levels after treatment with azitromicina
Time Frame
5 days
Title
IL1b
Description
increasing in plasma levels after treatment with azitromicina
Time Frame
5 days
Title
IL2
Description
increasing in plasma levels after treatment with azitromicina
Time Frame
5days
10. Eligibility
Sex
All
Minimum Age & Unit of Time
1 Minute
Maximum Age & Unit of Time
72 Hours
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
preterm infants of less than 37 weeks of gestational age who have undergone mechanical ventilation within the first 72 hours of life
Exclusion Criteria:
Major congenital malformations or chromosomal syndromes Mothers carrying the HIV virus.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Rita de Cassia Silveira
Organizational Affiliation
Federal University of Rio Grande do Sul
Official's Role
Principal Investigator
12. IPD Sharing Statement
Plan to Share IPD
Undecided
Citations:
PubMed Identifier
32894857
Citation
Nunes CR, Procianoy RS, Corso AL, Silveira RC. Use of Azithromycin for the Prevention of Lung Injury in Mechanically Ventilated Preterm Neonates: A Randomized Controlled Trial. Neonatology. 2020;117(4):522-528. doi: 10.1159/000509462. Epub 2020 Sep 7.
Results Reference
derived
Learn more about this trial
Azithromycin in the Prevention of Lung Injury in Premature Newborn
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