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Oklahoma city, Oklahoma 73104


Purpose:

Despite the lack of trials proving the efficacy of DNase in non cystic fibrosis patients, it is currently heavily used in this population. In fact, per evidence of barcode scanning via Meditech computer system at OU Medical Center 93% of the DNase prescribed in 2005 was for non Cystic fibrosis patients with an estimated yearly cost of $341,968.15.In vitro studies showed that the effect of Dnase was minimal on sputum viscosity when compared to Hypertonic saline . Furthermore recent studies on hypertonic saline in cystic fibrosis patients showed that it is an inexpensive and safe therapy when preceded by a bronchodilator in patients with cystic fibrosis. We hereby propose a prospective randomized trial to compare the efficacy of hypertonic saline, DNase, vs. normal saline in the treatment of atelectasis in non cystic fibrosis, mechanically ventilated patient.


Criteria:

Inclusion Criteria: 1. Patient on invasive mechanical ventilation 2. New Onset (<48 hours) lobar or multilobar lung atelectasis based on CXR Exclusion Criteria: 1. Asthma 2. Severe COPD (FEV1<30%) 3. Pneumothorax or massive pleural effusion, thought to be causing the atelectasis 4. Lobar atelectasis secondary to compressive tumor. 5. Severe hypoxemia (PaO2/FiO2 < 75) 6. Hemodynamic Instability 7. Cystic fibrosis patients 8. Allergy to DNase 9. Patients on Acetylcysteine 10. Pregnant women


NCT ID:

NCT00671723


Primary Contact:

Principal Investigator
Jean Keddissi, MD
University of Oklahoma


Backup Contact:

N/A


Location Contact:

Oklahoma city, Oklahoma 73104
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: January 21, 2018

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