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

This study has been completed.
Sponsor:
Information provided by (Responsible Party):
Sirilak Suksompong, Mahidol University
ClinicalTrials.gov Identifier:
NCT01725464
First received: November 8, 2012
Last updated: August 16, 2013
Last verified: August 2013
  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: Endpoint Classification: Safety/Efficacy Study
Intervention Model: Single Group Assignment
Masking: 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 Mahidol University:

Primary Outcome Measures:
  • Mean oxygen saturation at 30 minutes postoperative [ Time Frame: 30 minutes ] [ Designated as safety issue: Yes ]

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

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

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
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
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Please refer to this study by its ClinicalTrials.gov identifier: NCT01725464

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

No publications provided

Responsible Party: Sirilak Suksompong, Associate Profesor, Mahidol University
ClinicalTrials.gov Identifier: NCT01725464     History of Changes
Other Study ID Numbers: 541/2555(EC)
Study First Received: November 8, 2012
Last Updated: August 16, 2013
Health Authority: Thailand: Ethical Committee

Keywords provided by Mahidol University:
thoracotomy
oxygen saturation
postoperative

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

ClinicalTrials.gov processed this record on August 21, 2014