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NCT01725464 Clinical Trial

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

Hypoxia Clinical Trial

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

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT01725464
Other study ID # 541/2555(EC)
Secondary ID
Status Completed
Phase Phase 4
First received November 8, 2012
Last updated August 16, 2013
Start date November 2012
Est. completion date August 2013

Study information
Verified date August 2013
Source Mahidol University
Contact n/a
Is FDA regulated No
Health authority Thailand: Ethical Committee
Study type Interventional

Clinical Trial 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

Recruitment information / eligibility
Status Completed
Enrollment 34
Est. completion date August 2013
Est. primary completion date August 2013
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility 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

Study Design

Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Intervention

Device:
• oxygen cannular
Patient receives oxygen supplementation 5 LPM via oxygen cannular for 120 minutes after the operative

Locations
Country Name City State
Thailand Sirilak Suksompong Bangkok

Sponsors (1)
Lead Sponsor Collaborator
Mahidol University

Country where clinical trial is conducted

Thailand, 

Outcome
Type Measure Description Time frame Safety issue
Primary Mean oxygen saturation at 30 minutes postoperative 30 minutes Yes
Secondary incidence of oxygen saturation < 95% between 120 minutes until 3 days postoperative 3 days Yes
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