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The Use of LMA-Proseal and Endobronchial Blocker for One Lung Anesthesia, Case Series

M

Mahidol University

Status

Completed

Conditions

One-lung Ventilation
Anesthetic Technique

Treatments

Device: Bronchial blocker (Coopdech, Arndt)
Device: LMA-ProsealTM

Study type

Observational

Funder types

Other

Identifiers

NCT02106273
Si154/2011

Details and patient eligibility

About

An observational pilot study to determine the success rate of using LMA Proseal in conjuction with endobronchial blocker to provide one-lung anesthesia for thoracic surgery.

Full description

The use of LMA has gained popularity secondary to benefits confirmed by many literatures. However, LMA is rarely used in thoracic surgery. To enable one-lung ventilation, the LMA need to be used with bronchial blocker. The use of this combination has been reported as a rescue technique in special clinical scenarios, i.e. patient with difficult airway. When used in patient with difficult airway, the LMA will be inserted until proper ventilation achieved, then endobronchial blocker will be subsequently placed through the LMA into the selected main bronchus. The success rate of the the bronchial blocker placement via properly placed LMA has never been studied. This pilot study was designed to evaluate the success rate, the quality of lung collapsed, the dislodgement or other associated problems including some minor complications i.e. postoperative dysphagia, sore throat hoarseness of voice.

Enrollment

29 patients

Sex

All

Ages

18 to 75 years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

  • thoracic surgery that needed one-lung ventilation Exclusion Criteria:patient with
  • Restrictive lung disease that needed positive pressure ventilation > 30 cm.H2O
  • Mass or hematoma in the mouth which obstruct LMA insertion
  • Emergency surgery
  • Pregnancy
  • Severe infection or active pulmaonary tuberculosis
  • Hemoptysis
  • Pulmonary nodule > 20 cm. or bronchilal pathology
  • Pneumonectomy or sleeve resection

Trial design

29 participants in 1 patient group

Bronchial blocker
Description:
Pilot study to enroll ASA class I-III patients age between 18-70 years who undergoes thoracic surgery which require one-lung ventilation.
Treatment:
Device: LMA-ProsealTM
Device: Bronchial blocker (Coopdech, Arndt)

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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