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Spontaneous breathing trial for Acute Respiratory Distress Syndrome
N/A
Waitlist Available
Led By Barbara Schmidt, MD, MSc
Research Sponsored by University of Pennsylvania
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be younger than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 36 weeks postmenstrual age
Awards & highlights
No Placebo-Only Group
Summary
The objective of this study is to determine whether use of the spontaneous breathing trial allows for earlier successful extubation of very low birth weight (VLBW) infants who are intubated for \>48 hours and have not yet been successfully extubated (extubated \>7 days).
Eligible Conditions
- Acute Respiratory Distress Syndrome
- Respiratory Distress Syndrome
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 36 weeks postmenstrual age
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~36 weeks postmenstrual age
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
time to successful extubation
Secondary study objectives
bronchopulmonary dysplasia
extubation failure rate
Awards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: Spontaneous breathing trialExperimental Treatment1 Intervention
The spontaneous breathing trial will determine the extubation readiness of the subject.
Group II: Usual careActive Control1 Intervention
Subjects will be extubated using usual care, without the use of the spontaneous breathing trial.
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Who is running the clinical trial?
University of PennsylvaniaLead Sponsor
2,081 Previous Clinical Trials
42,724,739 Total Patients Enrolled
Barbara Schmidt, MD, MScPrincipal InvestigatorUniversity of Pennsylvania
4 Previous Clinical Trials
8,118 Total Patients Enrolled
Ann-Johanna Giaccone, MDStudy DirectorUniversity of Pennsylvania
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