Trial of Iseganan in Prevention of Ventilator-Associated Pneumonia

Stopped early · Phase 2/Phase 3

Conditions studied: Pneumonia

In brief

This is a multinational, double-blind, placebo-controlled trial designed to assess whether iseganan, applied topically to the oral cavity, can prevent ventilator-associated pneumonia among patients who are intubated and mechanically ventilated and survive for up to 14 days.

Key facts

Study ID

NCT00118781

Run by

IntraBiotics Pharmaceuticals

People needed

900

Starts

2003-09-01

Expected to finish

2004-06-01

Last updated by the study team

2005-07-19

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Greater than or equal to 18 years of age
• Orally/nasally intubated and receiving mechanical ventilation for <24 hours prior to scheduled randomization and administration of the first dose of Study Drug, and in the judgment of the attending physician, expected to remain intubated and mechanically ventilated for at least 48 hours
• Expected to survive for at least 21 days and to remain at the investigational site and not transferred to another institution while intubated during the 21-day study period
• Willing and able to provide written informed consent, or if unconscious or have altered sensorium, have a surrogate provide written informed consent as approved by the institution
• Negative pregnancy test within 7 days prior to randomization if a female of childbearing potential (Negative pregnancy test results [urine or serum] obtained for reason other than the purposes of this study are acceptable.)

You may not qualify if…

• Current diagnosis of pneumonia (Patients currently receiving antibiotics for treatment of pneumonia and patients who meet the study definition of clinically defined pneumonia at the time of screening will be excluded.)
• Absolute neutrophil count less than 1000/mm3
• Human immunodeficiency virus infection with a last known CD4 count less than 500/mm3
• Recipient of organ transplantation and receiving immunosuppressive therapy
• Current hematologic malignancy
• Previously documented cystic fibrosis
• Severe cranio-facial trauma or other medical condition expected to require imminent tracheostomy
• Patient, patient's family and/or physician not in favor of aggressive medical management or presence of an advanced directive to withhold life-sustaining treatment
• Moribund state or expected to survive less than 21 days due to an uncorrectable medical condition
• Participation in a clinical trial of any unlicensed drug, biologic or device within 30 days prior to the first dose of study drug
• Concurrent participation in a clinical trial of any unlicensed drug, biologic or device.

Where it is running

• Barnes-Jewish Hospital — St Louis, Missouri, United States

Full record on ClinicalTrials.gov

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