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Sponsored by: |
National Heart, Lung, and Blood Institute (NHLBI) |
Information provided by: | National Heart, Lung, and Blood Institute (NHLBI) |
ClinicalTrials.gov Identifier: | NCT00000574 |
To determine the effects of ibuprofen on mortality, development and reversal of shock, and adult respiratory distress syndrome, and on Lung Parenchymal Injury Score in adult patients with serious infection.
Condition | Intervention | Phase |
Acute Respiratory Distress Syndrome Lung Diseases Shock, Septic |
Drug: ibuprofen |
Phase III |
MedlinePlus related topics: | Sepsis |
Drug Information available for: | Ibuprofen Dexibuprofen |
Study Type: | Interventional |
Study Design: | Treatment, Randomized, Double-Blind, Placebo Control |
Study Start Date: | September 1990 |
Estimated Study Completion Date: | July 1995 |
Show Detailed Description |
Ages Eligible for Study: | 18 Years to 75 Years |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | No |
Men and women patients with known or suspected sites of serious infection if core temperature was 38.3 degrees Celsius, heart rate 90 in the absence of beta-blockers, respiratory rate 20 or minute ventilation 10 liters per minute. In addition, one o
Study ID Numbers: | 212 |
First Received: | October 27, 1999 |
Last Updated: | June 23, 2005 |
ClinicalTrials.gov Identifier: | NCT00000574 |
Health Authority: | United States: Federal Government |
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