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Ultrasound-guided Supine Anterior Thoracic Paravertebral Nerve Block for Postoperative Analgesia in Thoracoscopic Surgery: A Clinical Study

Ultrasound-guided Supine Anterior Thoracic Paravertebral Nerve Block for Postoperative Analgesia in Thoracoscopic Surgery: A Clinical Study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600123684
Enrollment
Unknown
Registered
2026-04-28
Start date
2025-01-04
Completion date
Unknown
Last updated
2026-05-04

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

Conditions

Post-thoracoscopic pain

Interventions

observation group:Ultrasound-guided anterior thoracic paravertebral block in the supine position
control group:Ultrasound-guided conventional approach thoracic paravertebral block

Sponsors

The First People's Hospital of Fuzhou City
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Patients who consent to participate in this trial protocol; 2. Patients undergoing elective thoracoscopic surgery; 3. Male or female, aged 18 to 65 years; 4. Body mass index (BMI) ranging from 18 to 28 kg/m²; 5. American Society of Anesthesiologists (ASA) physical status classification Grade ? to ?.

Exclusion criteria

Exclusion criteria: 1. Patients with cognitive or mental disorders who are unable to cooperate; 2. Patients with coagulation dysfunction; 3. Patients with infection or tumor at the puncture site; 4. Patients with severe hepatic and renal insufficiency (Child-Pugh Class C or eGFR < 30 mL/min/1.73m²); 5. Patients with a previous history of chronic neuropathic pain; 6. Patients with a history of illicit drug use; 7. Patients with a history of allergy to study-related drugs such as ropivacaine; 8. Patients refusing postoperative analgesia.

Design outcomes

Primary

MeasureTime frame
VAS score;postoperative nausea and vomiting;

Secondary

MeasureTime frame
nerve block puncture time;nerve block puncture depth;intraoperative remifentanil consumption;intraoperative propofol consumption;time of first pressing of patient-controlled intravenous analgesia pump;number of effective PCIA boluses within 48 h postoperatively;number of rescue analgesic administrations;serum interleukin-6 (IL-6);serum tumor necrosis factor-a (TNF-a);incidence of nerve block-related complications;respiratory depression;

Countries

China

Contacts

Public ContactLi Ming

The First People's Hospital of Fuzhou City

leesm23@sina.com+86 137 5593 6929

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 7, 2026