Trial record 1 of 3 for:
"Hemoperitoneum"
Effects of Hemoperitoneum Driven Carbon Monoxide on Post-Traumatic Stability and Platelet Aggregation
This study has been completed.
Sponsor:
The University of Texas Health Science Center at San Antonio
Information provided by (Responsible Party):
The University of Texas Health Science Center at San Antonio
ClinicalTrials.gov Identifier:
NCT01594034
First received: May 4, 2012
Last updated: May 11, 2012
Last verified: May 2012
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Purpose
Our objective is to determine whether or not the presence of hemoperitoneum in trauma patients is associated with increased Carbon Monoxide (CO) formation, and to determine if elevated Carbon Monoxide levels are associated with cardiovascular depression, impaired platelet aggregation, and/or multiple organ failure.
| Condition | Intervention |
|---|---|
| Hemoperitoneum | Procedure: expired air |
| Study Type: | Observational |
| Study Design: | Time Perspective: Prospective |
| Official Title: | Effects of Hemoperitoneum Driven Carbon Monoxide on Post-Traumatic Stability |
Further study details as provided by The University of Texas Health Science Center at San Antonio:
Primary Outcome Measures:
- •Establish a method for reliably measuring CO excretion in patients. [ Time Frame: 96 hours ]
| Enrollment: | 9 |
| Study Start Date: | November 2009 |
| Study Completion Date: | May 2011 |
| Primary Completion Date: | May 2011 (Final data collection date for primary outcome measure) |
| Groups/Cohorts | Assigned Interventions |
|---|---|
| no treatment |
Procedure: expired air
collection of expired air from ventilator
|
Eligibility| Ages Eligible for Study: | 18 Years and older (Adult, Senior) |
| Sexes Eligible for Study: | Female |
| Accepts Healthy Volunteers: | No |
| Sampling Method: | Probability Sample |
Study Population
patients in the ICU on a ventilator
Criteria
Inclusion Criteria:
- Hospitalized males 18 years of age or older,
- Diagnosis of isolated blunt OR blunt and penetrating trauma,
- Admitted or expecting to be admitted to the Intensive Care Unit,
- On mechanical ventilation, and
- Written informed consent obtained
Exclusion Criteria:
- Female gender, (Females will be excluded from this study as the menstrual cycle and other estrogen variations are known to be associated with cyclic changes in CO production adding a potential confounder to the interpretations of our findings.)
- Diagnosis of isolated penetrating trauma,
- Acute hemothorax or pneumothorax,
- Treatment with antiaggregants (ASA, clopidogrel, aggrenox or ticlopidine),
- Enrollment in another research study,
- Prisoners,
- Inability to perform CO measurement within 96 hours after hospital admission.
Contacts and Locations
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To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below.
For general information, see Learn About Clinical Studies.
Please refer to this study by its ClinicalTrials.gov identifier: NCT01594034
Please refer to this study by its ClinicalTrials.gov identifier: NCT01594034
Locations
| United States, Texas | |
| University Hospital | |
| San Antonio, Texas, United States, 78229 | |
Sponsors and Collaborators
The University of Texas Health Science Center at San Antonio
Investigators
| Principal Investigator: | Robert Johnson, PhD | University of Texas |
More Information
| Responsible Party: | The University of Texas Health Science Center at San Antonio |
| ClinicalTrials.gov Identifier: | NCT01594034 History of Changes |
| Other Study ID Numbers: |
HSC-2009-0176-H |
| Study First Received: | May 4, 2012 |
| Last Updated: | May 11, 2012 |
Additional relevant MeSH terms:
|
Hemoperitoneum Peritoneal Diseases Digestive System Diseases Hemorrhage Pathologic Processes Carbon Monoxide |
Antimetabolites Molecular Mechanisms of Pharmacological Action Gasotransmitters Neurotransmitter Agents Physiological Effects of Drugs |
ClinicalTrials.gov processed this record on July 14, 2017


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