The effect of emergence FIO2 on postoperative lung volume

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

CRIS

Registry ID

KCT0002642

Enrollment

Registered

2018-01-09

Start date

2017-05-22

Completion date

Unknown

Last updated

2019-03-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Others(FIO2 at anesthesia emergence) : Following the application of recovery FIO2 (100&#37

, 80&#37

or 40&#37

) to the patient according to the oxygen fraction assigned by the random table, we will observe and record perioperative changes in lung volume.

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: 18-80 aged, ASA I-III patients undergoing elective laparascopic abdominal surgery

Exclusion criteria

Exclusion criteria: 1) patients who can not be applied the sensors of EIT device 2) any abnomality in diaphragmatic function 3) patients with any pace maker 4) hemodynamic instability during the perioperative period, who transferred to postoperative ICU 5) A woman in pregnancy 6) Obese patient with BMI over 30- 7) any neuromuscular disease patient 8) preoperative active or chronic lung disease (chronic obstructive pulmonary disease, pneumonia, asthma) 9) predicted airway difficulty 10) patient who refuse to enroll to the study 11) emergency operation

Design outcomes

Primary

Measure	Time frame
perioperative lung volume change according to the applied FIO2 at anesthesa emergence	—

Secondary

Measure	Time frame
postoperative atelectasis	—

Countries

Korea, Republic of

Contacts

Public ContactJeong Jin Min

Samsung Medical Center

prudence2@hanmail.net+82-2-3410-2467

Outcome results