Actively Recruiting
Intraoperative Paravertebral Block and Postoperative Complications
Led by Tongji Hospital · Updated on 2025-10-08
500
Participants Needed
1
Research Sites
196 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This study aims to evaluate the clinical association between intraoperative paravertebral block and the reduction of postoperative complications following thoracic surgery.
CONDITIONS
Official Title
Intraoperative Paravertebral Block and Postoperative Complications
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Male or female participants aged 18 years or older
- Scheduled for 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 before participating in the study
You will not qualify if you...
- Patients who refuse to provide informed consent
- Anesthesiologists without training in ultrasound-guided paravertebral block (PVB-US)
- History of thoracic surgery on the same side
- Conversion to open thoracotomy during surgery
- Incomplete scheduled surgery due to disease progression or medical reasons
- Patients lost to follow-up or refusing postoperative follow-up
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Tongji Medical College of HUST: Huazhong University of Science and Technology Tongji Medical College Tongji Hospital
Wuhan, Hubei, China, 430000
Actively Recruiting
Research Team
G
Guo jiateng Guo
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
QUADRUPLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
PREVENTION
Number of Arms
2
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