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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01700088
Other study ID # 541/2555(EC2)
Secondary ID
Status Completed
Phase N/A
First received October 2, 2012
Last updated December 10, 2015
Start date November 2012
Est. completion date December 2013

Study information

Verified date December 2015
Source Mahidol University
Contact n/a
Is FDA regulated No
Health authority Thailand: Ethical Committee
Study type Observational

Clinical Trial 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.


Recruitment information / eligibility

Status Completed
Enrollment 35
Est. completion date December 2013
Est. primary completion date December 2013
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility 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

Study Design

Observational Model: Case-Only, Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
Thailand Faculty of Medicine, Siriraj Hospital, Mahidol University Bangkok

Sponsors (1)

Lead Sponsor Collaborator
Mahidol University

Country where clinical trial is conducted

Thailand, 

Outcome

Type Measure Description Time frame Safety issue
Primary Oxygen saturation We continuously monitor oxygen saturation and record every 5 minutes for 30 minutes postoperative. 30 minutes Yes
Secondary Incidence of hypoxemia 3 days postoperative Yes
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