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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

Tracking Information
First Submitted Date October 2, 2012
First Posted Date October 4, 2012
Last Update Posted Date December 11, 2015
Study Start Date November 2012
Actual Primary Completion Date December 2013   (Final data collection date for primary outcome measure)
Current Primary Outcome Measures
 (submitted: October 2, 2012)
Oxygen saturation [ Time Frame: 30 minutes ]
We continuously monitor oxygen saturation and record every 5 minutes for 30 minutes postoperative.
Original Primary Outcome Measures Same as current
Change History
Current Secondary Outcome Measures
 (submitted: October 2, 2012)
Incidence of hypoxemia [ Time Frame: 3 days postoperative ]
Original Secondary Outcome Measures Same as current
Current Other Pre-specified Outcome Measures Not Provided
Original Other Pre-specified Outcome Measures Not Provided
 
Descriptive Information
Brief Title The Effect of Nasal Cannulae During the First 2 Hours Postoperative in Patient Undergoing Thoracotomy
Official Title The Effect of Nasal Cannulae During the First 2 Hours Postoperative in Patient
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.
Detailed Description Not Provided
Study Type Observational
Study Design Observational Model: Case-Only
Time Perspective: Prospective
Target Follow-Up Duration Not Provided
Biospecimen Not Provided
Sampling Method Non-Probability Sample
Study Population Patient undergoing lung resection surgery.
Condition
  • Hypoxia
  • Post Pulmonary Resection
Intervention Not Provided
Study Groups/Cohorts Oxygen cannular
After lung resection surgery,every patient will received supplementary oxygen 5 L/minutes via oxygen cannular for 120 minutes
Publications * Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Recruitment Information
Recruitment Status Completed
Actual Enrollment
 (submitted: October 2, 2012)
35
Original Estimated Enrollment Same as current
Actual Study Completion Date December 2013
Actual Primary Completion Date December 2013   (Final data collection date for primary outcome measure)
Eligibility 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
Sex/Gender
Sexes Eligible for Study: All
Ages 18 Years and older   (Adult, Older Adult)
Accepts Healthy Volunteers No
Contacts Contact information is only displayed when the study is recruiting subjects
Listed Location Countries Thailand
Removed Location Countries  
 
Administrative Information
NCT Number NCT01700088
Other Study ID Numbers 541/2555(EC2)
Has Data Monitoring Committee No
U.S. FDA-regulated Product Not Provided
IPD Sharing Statement Not Provided
Responsible Party Sirilak Suksompong, Mahidol University
Study Sponsor Mahidol University
Collaborators Not Provided
Investigators
Principal Investigator: Sirilak Suksompong, MD Mahidol University
PRS Account Mahidol University
Verification Date December 2015