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Efficacy of ultrasound guided serratus anterior plane block compared with thoracic paravertebral block on acute pain in video-assisted thoracoscopic surgery

Efficacy of ultrasound guided serratus anterior plane block compared with thoracic paravertebral block on acute pain in video-assisted thoracoscopic surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800017671
Enrollment
Unknown
Registered
2018-08-08
Start date
2018-08-24
Completion date
Unknown
Last updated
2018-08-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acute pain after video-assisted thoracoscopic surgery

Interventions

GS:Ultrasound guided serratus anterior plane block
GP:Ultrasound thoracic paravertebral block
G:General anesthesia alone

Sponsors

Shanghai Chest Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Written informed consent; 2. Aged >18 years; 3. ASA Physical Status =3; 4. Elective video-assisted thoracoscopic surgery under general anesthesia; 5. Surgery duration expected to last >30 minutes; 6. Planned hospitalization >3 days.

Exclusion criteria

Exclusion criteria: 1. Emergency surgery; 2. Known clinically cardiac-vascular diseases; 3. Pregnancy; 4. Illiteracy, unable to communicate, unable to perform the VAS Scoring; 5. Surgical change to open thoracotomy; 6. Previous thoracic surgeries; 7. Patients with infection and abnormal coagulation at the puncture site are not included in this study.

Design outcomes

Primary

MeasureTime frame
Pain assessment;The first onset significant pain postoperatively;

Secondary

MeasureTime frame
Intro-op opioid consumption;Intro-op propofol consumption;Rescue analgesics dose spent;Post-24h vomit-nausia score;Post-72h Satisfaction survey;Intro-op Hypotension;

Countries

China

Contacts

Public ContactYUWEI QIU

Shanghai Chest Hospital, Shanghai Jiaotong University

qiuy@ccf.org+86 13818825406

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 18, 2026