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Intra-tracheal Instillation of Budesonide to Prevent Chronic Lung Disease (STOPCLD)

Primary Purpose

Infant, Extremely Premature, Acute Lung Injury, Chronic Lung Disease of Prematurity

Status
Recruiting
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
Infants in the study group (S/B group) will receive surfactant 2.5 mls/kg and Budesonide 0.5 mg (1mL)
Infants in the control group (S/P group) receive placebo (Normal saline 1mL)
Sponsored by
University of Arizona
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Infant, Extremely Premature

Eligibility Criteria

undefined - 18 Hours (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Infants born at < 30+0/7 weeks (23+0 - 29+6/7) gestational age (GA) OR with preterm infants with a birth weight (BW) which is < 1500 gm AND if they have severe respiratory distress syndrome (RDS) (Clinical diagnosis based on the need for mechanical ventilation in preterm infant or if they have radiologic features of RDS along with need for positive distending airway pressure and fractional inspired oxygen (FiO2) > 0.3)

Exclusion Criteria:

  1. major congenital defects
  2. chromosomal abnormality
  3. pneumothorax
  4. Known surgical disease
  5. Known or suspected congenital heart disease
  6. Infant not considered viable by physician
  7. Severe sepsis / infections
  8. Likely to be extubated within the next 24 hours

Sites / Locations

  • University of ArizonaRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

S/B group- infants

S/P group- control / placebo comparator

Arm Description

Infants randomized to the study group (S/B group) will receive surfactant and Budesonide - 0.5 mg -1mL

Infants randomized to the control group (S/P group) will receive surfactant and placebo (Normal Saline -1mL)

Outcomes

Primary Outcome Measures

Change of combined inflammatory cytokines
Change in inflammatory cytokines /chemokines (interleukin-6, 8, 10 and Tumor Necrosis Factor α (TNF-α) levels

Secondary Outcome Measures

chronic lung disease
Supplemental oxygen requirement at 36 weeks corrected gestational age
Mortality
All cause mortality
Ventilator days
duration of ventilation
Neuro-developmental outcome
Composite Bailey III neuro-developmental score. Scores range overall from 40 to 160 and for Cognitive: 55-145; Language: 47-153; Motor: 46-154; Social-Emotional: 55-145 with lower score for poor outcome and higher score for better outcome

Full Information

First Posted
May 2, 2022
Last Updated
October 31, 2022
Sponsor
University of Arizona
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1. Study Identification

Unique Protocol Identification Number
NCT05364385
Brief Title
Intra-tracheal Instillation of Budesonide to Prevent Chronic Lung Disease
Acronym
STOPCLD
Official Title
Intra-tracheal Instillation of Budesonide Along With Surfactant in Preterm Infants to Prevent Chronic Lung Disease
Study Type
Interventional

2. Study Status

Record Verification Date
October 2022
Overall Recruitment Status
Recruiting
Study Start Date
December 2, 2019 (Actual)
Primary Completion Date
February 2023 (Anticipated)
Study Completion Date
December 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Arizona

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Preterm infants are randomized to received either Intra-tracheal instillation of budesonide using surfactant as vehicle or a placebo. Intra-tracheal instillation of budesonide using surfactant as vehicle would facilitate its delivery to the periphery of the lung and would inhibit lung inflammation and mitigate acute lung injury.
Detailed Description
In extremely premature infants who are ventilated there is ongoing lung injury & lung inflammation. This can perpetuate the need for ongoing ventilation and these infants spend much longer in the hospital. The likelihood of chronic lung disease in this susceptible group is very high and they would need oxygen at home. Surfactant instillation has reduced the need for prolonged mechanical ventilation and to an extent the incidence of chronic lung disease (CLD). But many infants develop CLD and need prolonged oxygen treatment, diuretics and inhaled steroids to suppress the inflammation and obstruction of the airways. Some of the severely affected infants need orally administered steroids. The Inestigators propose to provide a dose of steroids instilled along with the surfactant in the very first day of life so as to prevent the vicious and ongoing cascade of lung injury and inflammation. As it is a poorly absorbed steroid and as only one or two doses is proposed to be used there is no effects within the body and it works locally within the lung. This is hoped to reduce CLD and improve long term outcomes. The population most susceptible to CLD is the extreme preterm infant with RDS who needs mechanical ventilation soon after birth. One of the groups will receive the surfactant with saline and the other group will receive the surfactant along with topical steroid. The groups will be followed during the hospital stay. survival along with duration of ventilation, duration of hospital stay and oxygen needs are noted. To study the hoped for long term benefits the investigators would note the long term neuro-development - if they were followed as per hospital policy between 18 months and 26 months. Intra-tracheal instillation of budesonide using surfactant as vehicle would facilitate its delivery to the periphery of the lung and would inhibit lung inflammation.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Infant, Extremely Premature, Acute Lung Injury, Chronic Lung Disease of Prematurity, Budesonide

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
25 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
S/B group- infants
Arm Type
Experimental
Arm Description
Infants randomized to the study group (S/B group) will receive surfactant and Budesonide - 0.5 mg -1mL
Arm Title
S/P group- control / placebo comparator
Arm Type
Placebo Comparator
Arm Description
Infants randomized to the control group (S/P group) will receive surfactant and placebo (Normal Saline -1mL)
Intervention Type
Drug
Intervention Name(s)
Infants in the study group (S/B group) will receive surfactant 2.5 mls/kg and Budesonide 0.5 mg (1mL)
Other Intervention Name(s)
Pulmicort
Intervention Description
Infants in the study group (S/B group) will receive surfactant 2.5 mls/kg and Budesonide 0.5 mg (1mL)
Intervention Type
Drug
Intervention Name(s)
Infants in the control group (S/P group) receive placebo (Normal saline 1mL)
Intervention Description
Infants in the control group (S/P group) will receive surfactant 2.5 mls/kg and placebo (Normal saline 1mL)
Primary Outcome Measure Information:
Title
Change of combined inflammatory cytokines
Description
Change in inflammatory cytokines /chemokines (interleukin-6, 8, 10 and Tumor Necrosis Factor α (TNF-α) levels
Time Frame
4 weeks
Secondary Outcome Measure Information:
Title
chronic lung disease
Description
Supplemental oxygen requirement at 36 weeks corrected gestational age
Time Frame
36 weeks corrected gestational age (CGA)
Title
Mortality
Description
All cause mortality
Time Frame
upto 40 weeks corrected gestational age (CGA)
Title
Ventilator days
Description
duration of ventilation
Time Frame
Upto 40 weeks corrected gestational age (CGA)
Title
Neuro-developmental outcome
Description
Composite Bailey III neuro-developmental score. Scores range overall from 40 to 160 and for Cognitive: 55-145; Language: 47-153; Motor: 46-154; Social-Emotional: 55-145 with lower score for poor outcome and higher score for better outcome
Time Frame
18 - 26 months corrected postnatal age

10. Eligibility

Sex
All
Maximum Age & Unit of Time
18 Hours
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Infants born at < 30+0/7 weeks (23+0 - 29+6/7) gestational age (GA) OR with preterm infants with a birth weight (BW) which is < 1500 gm AND if they have severe respiratory distress syndrome (RDS) (Clinical diagnosis based on the need for mechanical ventilation in preterm infant or if they have radiologic features of RDS along with need for positive distending airway pressure and fractional inspired oxygen (FiO2) > 0.3) Exclusion Criteria: major congenital defects chromosomal abnormality pneumothorax Known surgical disease Known or suspected congenital heart disease Infant not considered viable by physician Severe sepsis / infections Likely to be extubated within the next 24 hours
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
R Kylat, MD
Phone
5206266627
Email
rkylat@arizona.edu
Facility Information:
Facility Name
University of Arizona
City
Tucson
State/Province
Arizona
ZIP/Postal Code
85719
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Joanna Schrader
Phone
520-626-6282
Email
jschrader@arizona.edu

12. IPD Sharing Statement

Plan to Share IPD
Undecided

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Intra-tracheal Instillation of Budesonide to Prevent Chronic Lung Disease

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