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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
Hospital de Clinicas de Porto Alegre
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Bronchopulmonary Dysplasia

Eligibility Criteria

1 Minute - 72 Hours (Child)All SexesAccepts Healthy Volunteers

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

    First Posted
    March 25, 2018
    Last Updated
    March 25, 2018
    Sponsor
    Hospital de Clinicas de Porto Alegre
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    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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