Lung Ultrasound in Preterm Infants

Sponsor
Phoenix Children's Hospital (Other)
Overall Status
Enrolling by invitation
CT.gov ID
NCT05925075
Collaborator
St. Joseph's Hospital and Medical Center, Phoenix (Other), MedStar Georgetown University Hospital (Other), Baylor Scott and White Health (Other), Children's Hospital Los Angeles (Other), LAC+USC Medical Center (Other)
150
1
23.5
6.4

Study Details

Study Description

Brief Summary

The goal of this observational study is to learn about the role of bedside lung ultrasound in infants born prematurely with breathing problems. The main question this study aims to answer is: Can bedside lung ultrasound performed in the first month of life predict the development of chronic lung disease in premature infants?

Condition or Disease Intervention/Treatment Phase
  • Diagnostic Test: Lung Ultrasound

Detailed Description

This is a multicenter study including preterm infants born less than 32 weeks gestational age and with a diagnosis of respiratory distress syndrome (RDS). Our primary aim is to determine the ability of lung ultrasounds performed in the first month of life to predict the development of bronchopulmonary dysplasia (BPD) at 36 weeks postmenstrual age.

Secondary aims will evaluate the association of lung ultrasound scores with the severity of hemodynamically significant patent ductus arteriosus (PDA) at time of diagnosis, as well as describe lung ultrasound changes pre and post-treatment with systemic steroid course.

Hypothesis:
  1. LUS scores would have a predictive ability to identify extreme preterm infants at risk of BPD with AUC>0.8.

  2. Higher LUS scores would correlate with higher severity of hemodynamically significant PDA.

  3. LUS scores are expected to be lower after the course of systemic steroids and with lower scores are expected to predict successful extubation following the course of systemic steroids.

Study Design

Study Type:
Observational
Anticipated Enrollment :
150 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Point of Care Lung Ultrasound in Preterm Infants With Respiratory Distress: A Multicenter Prospective Study
Actual Study Start Date :
Apr 17, 2023
Anticipated Primary Completion Date :
Apr 1, 2025
Anticipated Study Completion Date :
Apr 1, 2025

Arms and Interventions

Arm Intervention/Treatment
RDS

Infant born less than 32 weeks gestation with diagnosis of respiratory distress syndrome. Lung ultrasounds will be performed on day of life 7, 14, 21, 28 and at corrected gestational age of 36 weeks.

Diagnostic Test: Lung Ultrasound
Lung ultrasound to be performed at scheduled intervals as described in individual cohorts.

PDA

In addition to being less than 32 weeks gestation, subject can qualify for study and receive a lung ultrasound scan at time of echo diagnosis of patent ductus arteriosus (PDA).

Diagnostic Test: Lung Ultrasound
Lung ultrasound to be performed at scheduled intervals as described in individual cohorts.

Steroid

Aims are : A: To evaluate changes in LUS scores pre and post treatment with systemic steroid course. B: To evaluate the predictive ability of LUS for successful extubation following course of systemic steroids. Lung ultrasound scans will be done prior to initiation of post-natal steroid, day 1, day 3, day 7, day 10 of treatment and 1 week after steroid is discontinued.

Diagnostic Test: Lung Ultrasound
Lung ultrasound to be performed at scheduled intervals as described in individual cohorts.

Outcome Measures

Primary Outcome Measures

  1. Assess predictive ability of lung ultrasound scores in infants at risk of developing bronchopulmonary dysplasia (BPD) [The lung ultrasounds will be performed on day of life 7, 14, 21 and 28 and diagnosis of BPD would be per standard criteria.]

    The primary outcome is to assess accuracy measures including specificity, sensitivity and area under ROC of lung ultrasound cut offs for predicting BPD.

Secondary Outcome Measures

  1. Association between lung ultrasound scores and severity of patent ductus arteriosus. [The lung ultrasound would be performed around the time of echocardiographic diagnosis of patent ductus arteriosus and severity determined by standard criteria.]

    Secondary outcome is to assess correlation between lung ultrasound scores and severity of patent ductus arteriosus.

  2. Comparison of lung ultrasound scores pre and post systemic steroid course administration [The lung ultrasound would be performed prior to steroid administration, 24 hours, 72 hours, 7 days, 10 days and 17 days after the first dose of 10 day course of systemic steroid administration.]

    Comparison of lung ultrasound scores prior to and after course of systemic steroid administration would be analyzed using paired T-test or the signed Wilcoxon rank sum test.

Eligibility Criteria

Criteria

Ages Eligible for Study:
0 Days and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:

Infants born less than 32 weeks gestation and meet one or more of the below criteria A) Diagnosis of Respiratory Distress Syndrome B) Diagnosis of PDA C) Post-natal steroid treatment for the purpose of weaning off ventilation support

Exclusion Criteria:

Infants with critical congenital heart and lung conditions and those with genetic anomalies.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Phoenix Children's Phoenix Arizona United States 85016

Sponsors and Collaborators

  • Phoenix Children's Hospital
  • St. Joseph's Hospital and Medical Center, Phoenix
  • MedStar Georgetown University Hospital
  • Baylor Scott and White Health
  • Children's Hospital Los Angeles
  • LAC+USC Medical Center

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Hemananda Muniraman, Staff Physician, Phoenix Children's Hospital
ClinicalTrials.gov Identifier:
NCT05925075
Other Study ID Numbers:
  • 22-172
First Posted:
Jun 29, 2023
Last Update Posted:
Jun 29, 2023
Last Verified:
Jun 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Hemananda Muniraman, Staff Physician, Phoenix Children's Hospital
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jun 29, 2023