The type of double lumen endotacheal tube and postoperative complication

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

CRIS

Registry ID

KCT0000676

Enrollment

Registered

2013-02-15

Start date

2012-03-12

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

Medical Device : Patients were randomized to two groups : Tracho(T) group (n=30), Silbroncho(S) group(n=30). In patients undergone elective thoracic surgery, DLT corresponding each group was used and

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: 1) American socitety of anesthesiologists(ASA) class I~III patients 2) aged 20 to 65 years 3) scheduled for elective thoracoscopic lobectomy or wedge resection

Exclusion criteria

Exclusion criteria: 1)history of surgery or disease on upper airway 2)preoprative sore throat or hoarseness

Design outcomes

Primary

Measure	Time frame
sore throat	—

Secondary

Measure	Time frame
hoarseness	—

Countries

Korea, Republic of

Contacts

Public ContactWonjung Hwang

The Catholic University of Korea, Seoul St. Mary's Hospital

Outcome results