Status:

NOT_YET_RECRUITING

Thoracic Surgery Intercostal Block Trial With Liposomal vs. Hydrochloride Bupivacaine

Lead Sponsor:

Shanghai Pulmonary Hospital, Shanghai, China

Conditions:

Postoperative Pain, Acute

Lung Cancer

Eligibility:

All Genders

18-80 years

Phase:

NA

Brief Summary

This randomized controlled trial evaluates the analgesic effects of liposomal bupivacaine compared to bupivacaine hydrochloride in intercostal nerve block for patients undergoing thoracoscopic lung su...

Detailed Description

Background: Lung cancer surgery, even with minimally invasive thoracoscopy, causes significant postoperative pain in up to 62.9% of patients, potentially leading to complications and chronic pain. Int...

Eligibility Criteria

Inclusion

  • Scheduled for elective unilateral thoracoscopic (VATS) lung surgery
  • Age 18 to 80 years
  • American Society of Anesthesiologists (ASA) physical status I-III

Exclusion

  • Contraindication to local anesthetics (infection at puncture site, allergy to local anesthetics, coagulopathy or other bleeding risk)
  • Sensory abnormalities in the planned chest-wall surgical area
  • Hepatic dysfunction (ALT \> 50 U/L, AST \> 40 U/L, or total bilirubin ≥ 19 μmol/L) or renal dysfunction (serum creatinine \> 112 μmol/L, BUN \> 7.1 mmol/L, or dialysis within 28 days before surgery)
  • Pregnancy, breastfeeding, women of childbearing potential not using adequate contraception, or planning pregnancy during the study period
  • Preoperative opioid use, history of chronic pain, or history of opioid abuse
  • Refusal to provide informed consent

Key Trial Info

Start Date :

September 1 2025

Trial Type :

INTERVENTIONAL

Allocation :

ESTIMATED

End Date :

December 20 2025

Estimated Enrollment :

210 Patients enrolled

Trial Details

Trial ID

NCT07134660

Start Date

September 1 2025

End Date

December 20 2025

Last Update

September 5 2025

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Thoracic Surgery Intercostal Block Trial With Liposomal vs. Hydrochloride Bupivacaine | DecenTrialz