RecruitingNot Applicable

Intraoperative Paravertebral Block and Postoperative Complications

China500 participantsStarted 2025-03-25

Plain-language summary

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

Who can participate

Age range18 Years – 80 Years

SexALL

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Inclusion criteria

✓. 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. -

Exclusion criteria

✕. 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.
✕. Patients who did not complete the scheduled surgery due to disease progression or medical reasons.
✕. Patients who are lost to follow-up or refuse postoperative follow-up. -

What they're measuring

Postoperative Complications

Timeframe: 1 to 3 months postoperatively

Trial details

NCT IDNCT07211529

SponsorTongji Hospital

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2028-05-31

Contact for this trial

Guo jiateng Guo

18737552580 18737552580@163.com

View on ClinicalTrials.gov More Video-assisted Thoracoscopic Surgery (VATS) trials