Expired Study
This study is not currently recruiting Study Participants on ClinicalConnection.com. If you would like to find active studies please search for clinical trials.

Boston, Massachusetts 02115


Purpose:

The purpose of this trial is to test the hypothesis that at the end of 28 days, infants and children with acute lung injury treated with prone positioning would have more ventilator-free days than those treated with supine positioning.


Study summary:

Multicenter, randomized, controlled clinical trial conducted from August 28, 2001 to April 23, 2004, of 102 pediatric patients from 7 US pediatric intensive care units aged 2 weeks to 18 years who were treated with supine vs. prone positioning. Randomization was concealed and group assignment was not blinded. Patients were randomized to either supine or prone positioning within 48 hours of meeting acute lung injury criteria, with those patients in the prone group being positioned within 4 hours of randomization and remaining prone for 20 hours each day during the acute phase of their illness for a maximum of 7 days, after which they were positioned supine. Both groups were treated using lung protective ventilator and sedation protocols, extubation readiness testing, and hemodynamic, nutrition, and skin care guidelines.


Criteria:

Inclusion Criteria: - Age >42 weeks post-conceptual age and <18 years of age - On mechanical ventilation (defined as presence of an endotracheal/tracheostomy tube and currently using ventilator support) - All of the following in the same 48 hour period: - acute pulmonary parenchymal disease (i.e., chest radiograph report of diffuse bilateral pulmonary alveolar infiltrates) - mechanical ventilation for at least 1 hour and anticipated need to continue mechanical ventilation for at least 24 hours - at least one PaO2/FiO2 ratio <300 (adjusted for barometric pressure: if altitude > 1000m, then PaO2/FiO2 <= 300x(B.P./760), regardless of mean airway pressure) - functional arterial catheter for blood gas analysis Exclusion Criteria: - Persistent hypotension (defined as systolic blood pressure of 70mmHg+(2x age in years)); i.e. patients requiring either intravenous fluids and/or increases of additional cardiotonic medications every 2 hours - Active bleeding that requires ongoing blood/fluid volume replacement - Currently on extracorporeal membrane oxygenation (ECMO) - Severe chronic lung disease (cystic fibrosis or bronchopulmonary dysplasia) - Respiratory failure presumed to be the result of cardiac disease - History of symptomatic or uncorrected congenital heart disease or a right to left intracardiac shunt - Bone marrow or lung transplant - Current known diagnosis of any of the following: - upper airway disease (i.e., tracheitis, tracheomalacia) - reactive airway disease (receiving beta agonists or acute doses of systemic corticosteroids) - refractory cerebral hypertension (intracranial pressure [ICP] >20mmHg for 1 hr) - neuromuscular respiratory failure (chronic assisted ventilation) - spinal instability (uncleared cervical spine) - unstable long bone fractures - Nonpulmonary condition that may be exacerbated by the prone position (for example, osteogenesis imperfecta, craniofacial surgery in the past week) - Draining abdominal surgical wound - Pregnancy - Subject's family/medical team have decided not to provide full support (patient treatment considered futile) - Enrollment in any other clinical trial within the last 30 days


NCT ID:

NCT00133614


Primary Contact:

Principal Investigator
Martha Curley, RN,PhD,FAAN
Children's Hospital Boston


Backup Contact:

N/A


Location Contact:

Boston, Massachusetts 02115
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: December 18, 2017

Modifications to this listing: Only selected fields are shown, please use the link below to view all information about this clinical trial.


Click to view Full Listing

This study is not currently recruiting Study Participants on ClinicalConnection.com. The form below is not enabled.