Liposomal and Standard Bupivacaine in Thoracic Paravertebral Block for Post-Thoracoscopic Pain (NCT06165991) | Clinical Trial Compass
RecruitingPhase 4
Liposomal and Standard Bupivacaine in Thoracic Paravertebral Block for Post-Thoracoscopic Pain
China496 participantsStarted 2024-06-01
Plain-language summary
I. Research purpose
1.1 Main Objective: To investigate the efficacy and safety of bupivacaine liposome thoracic paravertebral nerve block for postoperative analgesia after thoracoscopic lobectomy
1.2 Exploratory Objective: To investigate the noninferiority of bupivacaine liposomes in thoracic paravertebral nerve block with standard bupivacaine
Who can participate
Age range18 Years
SexALL
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* 1\) Age ≥18 years old;
2\) Patients undergoing unilateral initial thoracoscopic lobectomy under general anesthesia (TV or robot-assisted);
3\) American Society of Anesthesiologists (ASA) Grade I - III;
4\) Voluntarily participate in the study and sign the informed consent.
Exclusion Criteria:
* 1\) Pregnant or lactating women;
2\) Pulmonary wedge-shaped resection;
3\) ≥2 thoracic drainage tubes;
4\) Abnormal liver function: ALT and/or AST\>2Ă—ULN, or
TBIL≥1.5×ULN;
5\) Renal function impairment (serum creatinine \>176ÎĽmol/L), or received dialysis treatment within 28 days before surgery;
6\) Participate in another research trial involving an investigational drug within 6 months;
7\) A history of drug or alcohol abuse;
8\) Long-term use of opioids (more than 3 months or more than 5 mg daily morphine equivalent per day for 1 month);
9\) History of allergy to local anesthetics or one of the investigational drugs;
10\) Uncontrolled mental or neurological symptoms.