Calfactant
DrugEndotracheal calfactant, up to 3 doses if subject qualifies
NCT Number: NCT00999713
Acute lung injury (ALI) is a common, life-threatening complication among pediatric leukemia and lymphoma and hematopoietic stem cell transplant (HSCT) recipients. Although these children represent a relatively small and unique patient population, they account for the largest proportion of deaths of all pediatric diseases. The long-term goal of this project is to improve outcomes among these patients. Recently, the intratracheal administration of calfactant has resulted in decreased mortality among children with ALI including promising results among children with cancer and following HSCT. Consequently, the primary specific aim of this study is to assess the effect of calfactant on intensive care (PICU) survival among pediatric leukemia and lymphoma and HSCT patients with ALI. Secondary aims include assessment of the effect of calfactant on oxygenation and on the length of mechanical ventilation, PICU stay, and hospital stay. Calfactant therapy has been found to be of benefit in acute lung injury in the overall pediatric population by improving oxygenation and decreasing mortality. These findings, in conjunction with recent subgroup analysis in which calfactant therapy appeared to improve outcomes in immunocompromised children provide the rationale for assessing calfactant therapy in this patient population.
Funding Source - FDA Office of Orphan Products Development (OOPD)
Looking for future studies?
Notify Me18 month–21 year
All sexes
Interventional
Phase 2 / Phase 3
Hospital Sainte Justine, Montreal, Quebec, Canada
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Endotracheal calfactant, up to 3 doses if subject qualifies
Endotracheal air administration
Time frame: Admission to PICU discharge, up to 120 days
Overall mortality rate from admission to PICU discharge
Time frame: 60 days after study enrollment
Number of days the patient is alive and off of the ventilator
Time frame: Admission to discharge, up to 120 days
Length of stay (LOS) ,measured in days, from admission to PICU discharge and admission to hospital discharge.
Time frame: 48 hours after enrollment, up to 12 hours after each intervention
The Oxygenation Index after the first intervention is calculated as the fraction of inspired oxygen, in percent, times the mean airway pressure, in mmHg, divided by the partial pressure of oxygen in arterial blood, in mmHg. Lower values are better.
Time frame: 48 hours after enrollment, up to 12 hours after each intervention
The Oxygenation Index after the second intervention (if applicable) is calculated as the fraction of inspired oxygen, in percent, times the mean airway pressure, in mmHg, divided by the partial pressure of oxygen in arterial blood, in mmHg. Lower values are better.
Milton S. Hershey Medical Center
Other
A Phase 3 Trial of Calfactant for ALI in Pediatric Leukemia and HSCT Patients
Acronym: CALIPSO
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT01304654
Acute Lung Injury, Acute Respiratory Distress Syndrome
São Paulo, Brazil
View Trial DetailsNCT05825534
Acute Lung Injury, Acute Respiratory Distress Syndrome
Amiens, France
View Trial DetailsNCT04935697
Acute Lung Injury, Acute Lung Injury/Acute Respiratory Distress Syndrome (ARDS)
Pittsburgh, Pennsylvania, United States
View Trial DetailsNCT00963066
Acute Lung Injury, Lung Diseases
Caen, France
View Trial Details