Application of thoracic approach paravertebral block in postoperative analgesia of thoracic surgery: a randomized controlled trial.

Application of thoracoscopic paravertebral block for analgesia after video-assisted thoracic surgery

Status

Recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2000034726

Enrollment

Unknown

Registered

2020-07-16

Start date

2020-07-15

Completion date

Unknown

Last updated

2020-07-20

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

Conditions

Thoracic tumor

Interventions

Group 1:Oral analgesic only

Group 2:patient controlled intravenous analgesia

Group 3:utrasound guided thoracic paravertebral block

Group 4:thoracoscopic (thoracic approach) paravertebral

Eligibility

Sex/Gender

All

Age

20 Years to 80 Years

Inclusion criteria

Inclusion criteria: Patients who required or agreed to thoracoscopic surgery, and agreed to participate in the study.

Exclusion criteria

Exclusion criteria: Those who had abnormal coagulation function, had neurological or muscular diseases, had a history of spinal deformity, fracture, trauma or surgery, had a history of thoracic aortic aneurysm, did not cooperate in the research process or asked to withdraw.

Design outcomes

Primary

Measure	Time frame
Pain score;	—

Secondary

Measure	Time frame
Inflammatory factors;	—

Countries

China

Contacts

Public ContactLihong Hu

Ningbo Medical Center Lihuili Hospital

hlh_2000@163.com+86 13586584415

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 16, 2026