Intraoperative Paravertebral Block and Postoperative Complications

ConditionsVideo-assisted Thoracoscopic Surgery (VATS)Lung Cancer (Diagnosis)Pulmonary Infections Respiratory Failure Without Hypercapnia Pleural Effusion Due to Another Disorder (Disorder)Atelectasis Bronchospasm Pneumothorax Pulmonary Embolism (Diagnosis)Bronchopleural Fistula Acute Respiratory Distress Syndrome (ARDS)

Trial statusRecruiting

Trial phaseNot applicable

Trial typeInterventional

Biological sexAll

Age18-80

SponsorTongji Hospital

About this trial

This study aims to evaluate the clinical association between intraoperative paravertebral block and the reduction of postoperative complications following thoracic surgery.

Eligibility criteria

Qualifiers

Male or female participants aged 18 years or older.

Scheduled to undergo thoracic surgery via Video-Assisted Thoracoscopic Surgery (VATS) or Robotic-Assisted Thoracoscopic Surgery (RATS), including wedge resection, segmentectomy, lobectomy, or mediastinal surgery.

Signed informed consent obtained prior to study participation. -

Disqualifiers

Patients who refuse to provide informed consent.

Anesthesiologists who have not received training in ultrasound-guided paravertebral block (PVB-US).

History of ipsilateral thoracic surgery.

Conversion to open thoracotomy during the procedure.

Trial design

Treatments tested in this trial

Paravertebral Block (PVB)

Treatment groups

500 Participants

are divided into 2 treatment groups

Sponsors and collaborators

Tongji Hospital

Lead sponsor

Source ClinicalTrials.gov