- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01700088
The Effect of Nasal Cannulae During the First 2 Hours Postoperative in Patient Undergoing Thoracotomy
December 10, 2015 updated by: Sirilak Suksompong, Mahidol University
The Effect of Nasal Cannulae During the First 2 Hours Postoperative in Patient
At our institute,during the first 2 hour postoperative, we used to give supplement oxygen via face mask in patient having lung resection surgery.
After then if the patient is fine, we'll replace the face mask with nasal cannular untie the next morning.
We hypothesized that oxygen mask can be replace by nasal cannular without any hypoxia.
Study Overview
Status
Completed
Conditions
Study Type
Observational
Enrollment (Actual)
35
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Bangkok, Thailand, 10700
- Faculty of Medicine, Siriraj Hospital, Mahidol University
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (ADULT, OLDER_ADULT)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Patient undergoing lung resection surgery.
Description
Inclusion Criteria:
- age >/= 18 years old
- Patient undergoing lobectomy or pneumonectomy or wedge resection
- ASA 1-3
- Preoperative oxygen saturation < 95 %
Exclusion Criteria:
- Cannot communication
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
|---|
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Oxygen cannular
After lung resection surgery,every patient will received supplementary oxygen 5 L/minutes via oxygen cannular for 120 minutes
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Oxygen saturation
Time Frame: 30 minutes
|
We continuously monitor oxygen saturation and record every 5 minutes for 30 minutes postoperative.
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30 minutes
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Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Incidence of hypoxemia
Time Frame: 3 days postoperative
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3 days postoperative
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
November 1, 2012
Primary Completion (ACTUAL)
December 1, 2013
Study Completion (ACTUAL)
December 1, 2013
Study Registration Dates
First Submitted
October 2, 2012
First Submitted That Met QC Criteria
October 2, 2012
First Posted (ESTIMATE)
October 4, 2012
Study Record Updates
Last Update Posted (ESTIMATE)
December 11, 2015
Last Update Submitted That Met QC Criteria
December 10, 2015
Last Verified
December 1, 2015
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 541/2555(EC2)
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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