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

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT01725464
First Posted: November 12, 2012
Last Update Posted: August 19, 2013
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by (Responsible Party):
Sirilak Suksompong, Mahidol University
  Purpose
During early postoperative after lung resection surgery, patients without oxygen supplementation may experience hypoxemia. Oxygen supplementation can be given via oxygen mask or cannular. In this study the investigators want to the sudy the effect of oxygen supplementation via oxygen cannular during the first 120 minutes after surgery

Condition Intervention Phase
Lung Surgery Hypoxia Postoperative Device: oxygen cannular Phase 4

Study Type: Interventional
Study Design: Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: The Effect of Nasal Cannula During the First 2 Hours Postoperative in Patient Undergoing Thoracotomy

Resource links provided by NLM:


Further study details as provided by Sirilak Suksompong, Mahidol University:

Primary Outcome Measures:
  • Mean oxygen saturation at 30 minutes postoperative [ Time Frame: 30 minutes ]

Secondary Outcome Measures:
  • incidence of oxygen saturation < 95% between 120 minutes until 3 days postoperative [ Time Frame: 3 days ]

Enrollment: 34
Study Start Date: November 2012
Study Completion Date: August 2013
Primary Completion Date: August 2013 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: oxygen cannular
Patient receives oxygen supplementation 5 LPM via oxygen cannular for 120 minutes after the operative
Device: oxygen cannular
Patient receives oxygen supplementation 5 LPM via oxygen cannular for 120 minutes after the operative

  Eligibility

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • age =/> 18 years
  • lobectomy or pneumonectomy or wedge resection
  • ASA 1-3
  • preoperative oxygen saturation < 95 %
  • receiving epidural analgesia

Exclusion Criteria:

- cannot communication

  Contacts and Locations
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): NCT01725464


Locations
Thailand
Sirilak Suksompong
Bangkok, Thailand, 10700
Sponsors and Collaborators
Mahidol University
Investigators
Principal Investigator: Sirilak Suksompong, MD Mahidol University
  More Information

Responsible Party: Sirilak Suksompong, Associate Profesor, Mahidol University
ClinicalTrials.gov Identifier: NCT01725464     History of Changes
Other Study ID Numbers: 541/2555(EC)
First Submitted: November 8, 2012
First Posted: November 12, 2012
Last Update Posted: August 19, 2013
Last Verified: August 2013

Keywords provided by Sirilak Suksompong, Mahidol University:
thoracotomy
oxygen saturation
postoperative

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