NCT07211529Recruiting
Intraoperative Paravertebral Block and Postoperative Complications
Perioperative Paravertebral Block Reduces Postoperative Complications in Thoracic Surgery: An Observational Study
Source: ClinicalTrials.gov · Last updated 8 Oct 2025 · Not updated for over 12 months - ask the site whether it is still open
Brief summary (registry, in English)
This study aims to evaluate the clinical association between intraoperative paravertebral block and the reduction of postoperative complications following thoracic surgery.
- Status (registry)
- Recruiting
- Study type
- Interventional
- Enrollment
- 500 (estimated)
- First submitted
- 30 Sept 2025
- Start date
- 25 Mar 2025
- Primary completion date
- 31 May 2028
- Lead sponsor
- Tongji Hospital
- Diseases
- Lung cancer
- NCT number
- NCT07211529
What you commit to
- Study type: Interventional
- Planned participants: 500
- From 25 Mar 2025 to the primary completion date, 31 May 2028
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Anesthesiologists who have not received training in ultrasound-guided paravertebral block (PVB-US).
Other illness
- History of ipsilateral thoracic surgery.
- Patients who did not complete the scheduled surgery due to disease progression or medical reasons.
Other
- Patients who refuse to provide informed consent.
- Conversion to open thoracotomy during the procedure.
- Patients who are lost to follow-up or refuse postoperative follow-up. -
Who the study is looking for
- 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. -
Age in the registry: 18 years to 80 years · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Tongji Medical College of HUST: Huazhong University of Science and Technology Tongji Medical College Tongji Hospital Coordinator of this site? Confirm its status | Wuhan | China | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.