Use Of Capnography As Surrogate Measure Of PC02 In Medical Intensive Care Unit (ICU) Patients
This study has been terminated.
(Principal Investigator (central contact) has left the organization and requests the study be terminated)
Sponsor:
Lahey Clinic
Information provided by:
Lahey Clinic
ClinicalTrials.gov Identifier:
NCT00744614
First received: August 29, 2008
Last updated: October 19, 2010
Last verified: October 2010
| Tracking Information | |||||
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| First Received Date ICMJE | August 29, 2008 | ||||
| Last Updated Date | October 19, 2010 | ||||
| Start Date ICMJE | November 2007 | ||||
| Primary Completion Date | October 2010 (final data collection date for primary outcome measure) | ||||
| Current Primary Outcome Measures ICMJE |
PCO2 level [ Time Frame: 6 months ] [ Designated as safety issue: No ] | ||||
| Original Primary Outcome Measures ICMJE | Same as current | ||||
| Change History | Complete list of historical versions of study NCT00744614 on ClinicalTrials.gov Archive Site | ||||
| Current Secondary Outcome Measures ICMJE |
Time to intubation [ Time Frame: 6 months ] [ Designated as safety issue: No ] | ||||
| Original Secondary Outcome Measures ICMJE | Same as current | ||||
| Current Other Outcome Measures ICMJE | Not Provided | ||||
| Original Other Outcome Measures ICMJE | Not Provided | ||||
| Descriptive Information | |||||
| Brief Title ICMJE | Use Of Capnography As Surrogate Measure Of PC02 In Medical Intensive Care Unit (ICU) Patients | ||||
| Official Title ICMJE | Use Of Capnography As Surrogate Measure Of PC02 In Medical ICU Patients | ||||
| Brief Summary | The purpose of this study is to evaluate the use of Capnography (Continuous recording of the carbon dioxide content of expired air)as an alternative test to measure PC02 levels in patients with asthma, chronic obstructive pulmonary (COPD,interstitial lung disease(ILD)or coronary disease who are at risk of intubation. |
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| Detailed Description | This is a prospective study to evaluate the usefulness of capnography as a non-invasive, accurate method of measuring of PC02 levels in medical intensive care unit patients with asthma, COPD, ILD, or coronary disease who are at risk of intubation. |
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| Study Type ICMJE | Observational | ||||
| Study Design ICMJE | Observational Model: Cohort Time Perspective: Prospective |
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| Target Follow-Up Duration | Not Provided | ||||
| Biospecimen | Not Provided | ||||
| Sampling Method | Non-Probability Sample | ||||
| Study Population | MICU patients who are at risk of intubation and who have a history of asthma, COPD, ILD or coronary disease. |
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| Condition ICMJE |
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| Intervention ICMJE | Procedure: Capnography
A technique for monitoring the concentration or partial pressure of CO2 levels in respiratory gases |
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| Study Group/Cohort (s) | 1
Medical Intensive care unit patients with asthma, COPD, ILD or coronary disease who are at risk of intubation
Intervention: Procedure: Capnography |
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| Publications * | Török SS, Leuppi JD, Baty F, Tamm M, Chhajed PN. Combined oximetry-cutaneous capnography in patients assessed for long-term oxygen therapy. Chest. 2008 Jun;133(6):1421-5. Epub 2008 Mar 13. | ||||
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* Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline. |
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| Recruitment Information | |||||
| Recruitment Status ICMJE | Terminated | ||||
| Estimated Enrollment ICMJE | 70 | ||||
| Completion Date | October 2010 | ||||
| Primary Completion Date | October 2010 (final data collection date for primary outcome measure) | ||||
| Eligibility Criteria ICMJE | Inclusion Criteria:
Exclusion Criteria:
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| Gender | Both | ||||
| Ages | 18 Years and older | ||||
| Accepts Healthy Volunteers | No | ||||
| Contacts ICMJE | Contact information is only displayed when the study is recruiting subjects | ||||
| Location Countries ICMJE | United States | ||||
| Administrative Information | |||||
| NCT Number ICMJE | NCT00744614 | ||||
| Other Study ID Numbers ICMJE | 2007-115 | ||||
| Has Data Monitoring Committee | No | ||||
| Responsible Party | David Riker, M.D., Lahey Clinic, Inc. | ||||
| Study Sponsor ICMJE | Lahey Clinic | ||||
| Collaborators ICMJE | Not Provided | ||||
| Investigators ICMJE |
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| Information Provided By | Lahey Clinic | ||||
| Verification Date | October 2010 | ||||
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ICMJE Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP |
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