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

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.

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Key information

Conditions

Hypoxia Pathological Conditions, Signs and Symptoms Post Pulmonary Resection Signs and Symptoms Signs and Symptoms, Respiratory

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Faculty of Medicine, Siriraj Hospital, Mahidol University

Bangkok, 10700, Thailand

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Primary outcomes

Oxygen saturation

Time frame: 30 minutes

We continuously monitor oxygen saturation and record every 5 minutes for 30 minutes postoperative.

Secondary outcomes

Incidence of hypoxemia

Time frame: 3 days postoperative

Sponsors and collaborators

Lead sponsor

Mahidol University

Other

Registry information

Official study title

The Effect of Nasal Cannulae During the First 2 Hours Postoperative in Patient

Important dates

Study start: 2012
Primary completion: 2013
Study completion: 2013
First posted: Oct 4, 2012
Registry last updated: Dec 11, 2015

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.

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