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The Effect of Nasal Cannulae During the First 2 Hours Postoperative in Patient Undergoing Thoracotomy

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ClinicalTrials.gov Identifier: NCT01700088
Recruitment Status : Completed
First Posted : October 4, 2012
Last Update Posted : December 11, 2015
Sponsor:
Information provided by (Responsible Party):
Sirilak Suksompong, Mahidol University

Study Description
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Brief Summary:
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.

Condition or disease
Hypoxia Post Pulmonary Resection

Study Design
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Study Type : Observational
Actual Enrollment : 35 participants
Observational Model: Case-Only
Time Perspective: Prospective
Official Title: The Effect of Nasal Cannulae During the First 2 Hours Postoperative in Patient
Study Start Date : November 2012
Actual Primary Completion Date : December 2013
Actual Study Completion Date : December 2013

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Oxygen Therapy

Groups and Cohorts
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Group/Cohort
Oxygen cannular
After lung resection surgery,every patient will received supplementary oxygen 5 L/minutes via oxygen cannular for 120 minutes


Outcome Measures
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Primary Outcome Measures :
  1. Oxygen saturation [ Time Frame: 30 minutes ]
    We continuously monitor oxygen saturation and record every 5 minutes for 30 minutes postoperative.


Secondary Outcome Measures :
  1. Incidence of hypoxemia [ Time Frame: 3 days postoperative ]

Eligibility Criteria
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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
Patient undergoing lung resection surgery.
Criteria

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
Contacts and Locations
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Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01700088


Locations
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Thailand
Faculty of Medicine, Siriraj Hospital, Mahidol University
Bangkok, Thailand, 10700
Sponsors and Collaborators
Mahidol University
Investigators
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Principal Investigator: Sirilak Suksompong, MD Mahidol University
More Information
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Responsible Party: Sirilak Suksompong, Associate Professor, Mahidol University
ClinicalTrials.gov Identifier: NCT01700088    
Other Study ID Numbers: 541/2555(EC2)
First Posted: October 4, 2012    Key Record Dates
Last Update Posted: December 11, 2015
Last Verified: December 2015
Keywords provided by Sirilak Suksompong, Mahidol University:
hypoxemia
Post Pulmonary Resection
Additional relevant MeSH terms:
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Hypoxia
Signs and Symptoms, Respiratory