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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
Information provided by (Responsible Party):

Study Description
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

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
Primary Completion Date : December 2013
Study Completion Date : December 2013

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Oxygen Therapy
U.S. FDA Resources

Groups and Cohorts

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

Outcome Measures

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, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
Patient undergoing lung resection surgery.

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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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

Faculty of Medicine, Siriraj Hospital, Mahidol University
Bangkok, Thailand, 10700
Sponsors and Collaborators
Mahidol University
Principal Investigator: Sirilak Suksompong, MD Mahidol University
More Information

Responsible Party: Sirilak Suksompong, Associate Professor, Mahidol University
ClinicalTrials.gov Identifier: NCT01700088     History of Changes
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:
Post Pulmonary Resection

Additional relevant MeSH terms:
Signs and Symptoms, Respiratory
Signs and Symptoms