Correlation Between Carbon Dioxide Measured in End of Exhalation and Arterial Blood
This study is currently recruiting participants.
Verified July 2012 by Hospital Universitario Getafe
Sponsor:
Hospital Universitario Getafe
Information provided by (Responsible Party):
Susana Arias Rivera, Hospital Universitario Getafe
ClinicalTrials.gov Identifier:
NCT01646008
First received: July 18, 2012
Last updated: July 19, 2012
Last verified: July 2012
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Purpose
The purpose of this study is to study the correlation between carbon dioxide measured by capnography at the enf of exhalation and arterial blood in COPD patients with nasal cannula in critical care unit.
| Condition | Intervention |
|---|---|
|
Determine the Correlation Between Exhaled Carbon Dioxide and in Arterial Blood |
Other: To measure carbon dioxide by capnography and arterial blood Other: to measure carbon dioxide by capnography and arterial blood |
| Study Type: | Observational |
| Study Design: | Time Perspective: Prospective |
| Official Title: | Correlation Between Carbon Dioxide Measured in End of Exhalation and Arterial Blood in Chronic Obstructive Pulmonary Disease (COPD) in Intensive Care Unit With Nasal Cannula |
Resource links provided by NLM:
MedlinePlus related topics:
COPD (Chronic Obstructive Pulmonary Disease)
Drug Information available for:
Carbon dioxide
U.S. FDA Resources
Further study details as provided by Hospital Universitario Getafe:
| Estimated Enrollment: | 30 |
| Study Start Date: | July 2012 |
| Groups/Cohorts | Assigned Interventions |
|---|---|
| respiratory |
Other: To measure carbon dioxide by capnography and arterial blood
Three times per day will be measured exhaled carbon dioxide and obtained in arterial blood sample.
Other: to measure carbon dioxide by capnography and arterial blood
three times per day we will obtained arterial blood samples and measurements of carbon dioxide by capnography
|
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
| Sampling Method: | Non-Probability Sample |
Study Population
All adult COPD patients admitted to the ICU who consent
Criteria
Inclusion Criteria:
- Adults
- COPD patients
Exclusion Criteria:
- Under-aged
- Pregnant
- Major burns
Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT01646008
Contacts
| Contact: Susana Arias-Rivera, Graduate | 916839360 ext 2459 | sarias.hugf@salud.madrid.org |
| Contact: Maria M Sanchez Sanchez, graduate | 916839360 ext 2370 | marwestpot@yahoo.es |
Locations
| Spain | |
| Hospital Universitario de Getafe | Recruiting |
| Getafe, Madrid, Spain, 28905 | |
| Contact: Susana Arias-Rivera, Graduate 916839360 ext 2459 sarias.hugf@salud.madrid.org | |
Sponsors and Collaborators
Hospital Universitario Getafe
Investigators
| Principal Investigator: | Susana Arias-Rivera, Graduate | Hospital Universitario de Getafe, Spain |
More Information
No publications provided
| Responsible Party: | Susana Arias Rivera, Registered Nurse, Hospital Universitario Getafe |
| ClinicalTrials.gov Identifier: | NCT01646008 History of Changes |
| Other Study ID Numbers: | Carbon dioxide Getafe |
| Study First Received: | July 18, 2012 |
| Last Updated: | July 19, 2012 |
| Health Authority: | Spain: Comité Ético de Investigación Clínica |
Additional relevant MeSH terms:
|
Pulmonary Disease, Chronic Obstructive Lung Diseases, Obstructive Lung Diseases Respiratory Tract Diseases |
ClinicalTrials.gov processed this record on May 16, 2013