Diseases
Estimation of Intrinsic Positive End-Expiratory Pressure (PEEP) in Acute Respiratory Distress Syndrome (ARDS)
| Descriptive Information | |
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| Brief Title † | Estimation of Intrinsic Positive End-Expiratory Pressure (PEEP) in Acute Respiratory Distress Syndrome (ARDS) |
| Official Title † | |
| Brief Summary | ARDS (Acute Respiratory Distress Syndrome) is a condition of severe inflammation and excess fluids in the lungs that impairs their function of oxygen uptake to the point of needing a ventilator (breathing machine) to help them obtain enough oxygen into the body. Because of the high amounts of gas that the ventilator has to give to these patients, high pressures may develop deep into the lungs and produce complications for the patient. However, physicians sometimes cannot recognize it because it requires special equipment to measure pressure deep in the lungs. The goal of this study is to determine if the amount of this pressure can be calculated using mathematical formulas and the routine numbers provided by ventilators. The study consists on making the conventional measurement of this deep pressure and at the same time calculate this same pressure from other measurements that the ventilator routinely provides, to see if the calculated value can replace the more complicated conventional measurement. The measurements will be done by:
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| Detailed Description | |
| Study Phase | N/A |
| Study Type † | Observational |
| Study Design † | Time Perspective: Prospective |
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| Publications * | |
| * Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline. | |
| Recruitment Information | |
| Recruitment Status † | |
| Estimated Enrollment † | |
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| Eligibility Criteria † | Inclusion Criteria:
Exclusion Criteria:
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| Gender | Both |
| Ages | 18 Years - N/A |
| Accepts Healthy Volunteers | No |
| Contacts †† |
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| Location Countries † | United States, |
| Administrative Information | |
| NCT ID † | NCT00446706 |
| Organization ID | Estimation PEEPi |
| Secondary IDs †† | |
| Responsible Party | , |
| Study Sponsor † | Texas Tech University Health Sciences Center |
| Collaborators †† | |
| Investigators † | Principal Investigator: Juan Figueroa-Casas, MD, Texas Tech University Health Sciences Center |
| Information Provided By | Texas Tech University Health Sciences Center |
| Verification Date | May 2008 |
| First Received Date † | March 12, 2007 |
| Last Updated Date | May 23, 2008 |
†† WHO trial registration data element that is required only if it exists.