Brief Bronchial Suction for Lung Collapse During Uniportal VATS

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorMahidol University

About this trial

The goal of this clinical trial is to learn whether a brief suction of the airway going to the surgical lung (bronchus) can help the lung collapse faster and more completely during uniportal video-assisted thoracoscopic surgery (UVATS). This type of surgery is performed through a small incision in the chest, and good lung collapse helps the surgeon see and work safely. The main questions it aims to answer are

1. Does brief bronchial suction improve the quality of lung collapse 1 minute after chest cavity is opened? 2. Does brief bronchial suction help reach satisfactory lung collapse faster?

Researchers will compare patients who receive brief bronchial suction and those who do not. This is to see if suction improves and fastens lung collapse, reduce the need for additional steps if lung is not adequately collapsed, affect inflammation, oxygenation, postoperative pulmonary complications, operative time, and the duration of one-lung ventilation. Participants will

1. Undergo UVATS under general anesthesia 2. Have a double-lumen breathing tube placed as part of the standard anesthetic care 3. Be randomly assigned to either receive bronchial suction for one minute or receive no bronchial suction 4. Have the surgical team assess the quality of lung collapse at different time points 5. Have information collected from the routine anesthesia and surgical records such as oxygen levels during surgery, length of surgery and lung-related complications within 7 days after surgery

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Age ≥ 18 years old

BMI ≤ 35 kg/m2

American Society of Anesthesiologists (ASA) physical status I to III

Scheduled for elective single-port video-assisted thoracoscopic surgery (VATS) at Siriraj Hospital

Disqualifiers

Previous thoracic surgery

Known or suspected severe pleural adhesions based on preoperative imaging or clinical history

Tracheobronchial anatomical abnormalities

Pulmonary bullae identified on chest radiography or computed tomography, or a history of recurrent pneumothorax

Trial design

Design model

Parallel

Treatments tested in this trial

  • bronchial suction

    Other intervention

    Participants will receive bronchial suction at -30 cmH₂O through the bronchoscopy port of the operative lumen of the double-lumen endotracheal tube on two occasions: (1) during a 60-second apnea period immediately before initiation of one-lung ventilation and (2) during a 60-second apnea period immediately after pleural opening. Following the first suction period, the bronchoscopy port of the operative lumen will be closed. The bronchoscopy port of the operative lumen will be opened to ambient air following the second suction period after pleural entry.

  • Sham Control

    Other intervention

    Participants will undergo the same 60-second apnea periods as the bronchial suction group immediately before initiation of one-lung ventilation and immediately after pleural opening. The suction device will be activated for 60 seconds to produce sham suction noise but will not be connected to the patient.

Treatment groups

100 Participants
are divided into 2 treatment groups
Group A: Bronchial suctionExperimental treatment 1 intervention
Group B: No bronchial suctionSham comparator 1 intervention

Trial outcomes

Primary outcomes

1

Quality of lung collapse at 1 minute after pleural opening

Surgical team to assess quality of lung collapse at 1 minute after pleural opening by using lung collapse score (LCS). The higher the LCS, the better the lung collapse.

Time frame
At 1 minute after pleural opening

Secondary outcomes

1

Quality of lung collapse at pleural opening, 5 minutes and 10 minutes after pleural opening

Quality of lung collapse assessed by the surgical team using the Lung Collapse Score (LCS) immediately after pleural opening, and at 5 minutes and 10 minutes after pleural opening.

Time frame
At pleural opening, and at 5 and 10 minutes after pleural opening
2

Time to satisfactory lung collapse

Time from pleural opening to the first Lung Collapse Score (LCS) of 8 or greater

Time frame
From pleural opening until the first LCS of 8 or greater, assessed up to 10 minutes after pleural opening
3

Requirement for rescue maneuvers for inadequate lung collapse

Need for additional intraoperative maneuvers to improve lung collapse due to inadequate surgical exposure

Time frame
From pleural opening until the end of one-lung ventilation during the index surgery up to 6 hours
4

Incidence of intraoperative hypoxemia

Occurrence of intraoperative hypoxemia during one-lung ventilation, defined as SpO2 \< 90%

Time frame
From initiation of one-lung ventilation until resumption of two-lung ventilation during the index surgery up to 6 hours

Other outcomes

Sponsors and contacts

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