Comparison between costotransverse foramen block and thoracic paravertebral block before VATS pulmonary resection

Comparison between costotransverse foramen block and thoracic paravertebral block before VATS pulmonary resection: a randomized non-inferiority trial

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

CRIS

Registry ID

KCT0006704

Enrollment

Registered

2021-11-04

Start date

2021-11-24

Completion date

Unknown

Last updated

2025-07-21

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

Conditions

None listed

Interventions

Procedure/Surgery : As per randomized group allocation, perform either of the following blocks (thoracic paravertebral block or costotransverse block) after general anesthesia before the surgery start

proper anterior spreading of injectate fluid was adequately visualized in the ultrasound view) was observed to confirm the correct positioning of the needle. Subsequently, the remaining local anesthet

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: A. elective video-assisted thoracoscopic surgery pulmonary resection surgery B. 20 to 70 years of age C. American society of anesthesiologist (ASA) class 1 ~ 3

Exclusion criteria

Exclusion criteria: A. hypersensitivity to local anesthetics B. Wound infection or accompanying severe inflammation C. non-cooperative patient (unable to assess pain score) D. liver cirrhosis E. impaired renal function (estimated glomerular filtration rate <30 mL/min/1.73m2) F. non-minor pleural adhesion G. Known side effect to the analgesics involved in the study H. pregnancy I. known conflict of interest J. Previous intrathoracic surgery

Design outcomes

Primary

Measure	Time frame
area under the curve of the 24 hours pain score (NRS) graph	—

Secondary

Measure	Time frame
use of rescue analgesics ;postoperative nausea and vomiting;pulmonary function test (spirometer) ;quality of recovery-15;distribution of the nerve blockade;24 hours cumulative use of paitent controlled analgesia (fentanyl; mcg)	—

Countries

Korea, Republic of

Contacts

Public ContactChahyun Oh

Chungnam National University Hospital

5chahyun@naver.com+82-42-280-7840

Outcome results