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Clinical Trials/NCT01725464
NCT01725464CompletedPhase 4

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

Mahidol University2 sites in 1 country34 target enrollmentStarted: November 2012Last updated:
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Conditions

Trial Snapshot

Phase
Phase 4
Status
Completed
Enrollment
34
Locations
2
Primary Endpoint
Mean oxygen saturation at 30 minutes postoperative
Study OverviewStudy DesignEligibility CriteriaOutcomesInvestigatorsSitesRecords & IdentifiersSimilar Trials

Study Overview

Brief Summary

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

Study Design

Study Type
Interventional
Allocation
Na
Intervention Model
Single Group
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

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

Exclusion Criteria

  • •cannot communication

Outcomes

Primary Outcomes

Mean oxygen saturation at 30 minutes postoperative

Time Frame: 30 minutes

Secondary Outcomes

  • incidence of oxygen saturation < 95% between 120 minutes until 3 days postoperative(3 days)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Sirilak Suksompong

Associate Profesor

Mahidol University

Study Sites (2)

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The Effect of Nasal Cannula During the... | Clinical Trial