MedTrace Logo

Intraoperative Paravertebral Block and Postoperative Complications

NCT07211529 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 500

Last updated 2025-10-08

No results posted yet for this study

Summary

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

Conditions

  • Video-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)

Interventions

PROCEDURE

Paravertebral Block (PVB)

Participants in this arm will receive a paravertebral nerve block (PVB) performed intraoperatively under ultrasound guidance prior to the thoracic surgical procedure. The block will target the relevant thoracic vertebral levels corresponding to the surgical site. Standard local anesthetic agents will be administered according to institutional protocols. This intervention aims to provide perioperative analgesia, reduce postoperative pain, and potentially decrease the incidence of postoperative complications. All participants will also receive standard intraoperative monitoring and anesthesia management as per routine clinical practice.

Sponsors & Collaborators

  • Tongji Hospital

    lead OTHER

Principal Investigators

  • Zhang qin Zhang · Huazhong keji daxue tongji yixue yuan fushu tongji yiyuan

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
QUADRUPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-03-25
Primary Completion
2028-05-31
Completion
2028-12-31

Countries

  • China

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07211529 on ClinicalTrials.gov