Phase
Condition
Chronic Pain
Pain
Post-surgical Pain
Treatment
Liposomal bupivacaine
Bupivacaine Hydrochloride
Clinical Study ID
Ages > 18 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Participants who scheduled for elective video-assisted thoracoscopic lobectomy undergeneral anesthesia.
Participants were 18 years or older.
18 kg/m2≤BMI≤30 kg/m2
Participants with American Society of Anesthesiology (ASA) physical status I-III.
Understand the significance, possible benefits, potential risks of the trial indetail.Understand the procedures and methods of this study.Willing to complete thetrial in strict compliance with the clinical trial protocol.Sign the informedconsent form voluntarily.
Exclusion
Exclusion Criteria:
with severe cardiovascular and cerebrovascular diseases such as myocardialinfarction,unstable angina pectoris,severe cardiac rhythm disorders (second- andthird-degree heart block,etc.), New York Heart Association (NYHA) functional classIII/IV,Ischemic stroke.
with psychiatric disorders (such as schizophrenia,depression,etc.) and cognitiveimpairment.
with sensory disorders such as hyperalgesia.
with other bodily pain.
allergy to amide-type local anesthetics or any of the trial drugs
taking drugs that affect livermetabolism,corticosteroids,benzodiazepines,non-steroidal anti-inflammatorydrugs(NSAIDs),opioid agonist-antagonist,central-alpha 2-agonists,anticonvulsants,antidepressants within 72h.
with a history of alcohol or opioid abuse.
who were pregnant or lactating.
who were currently included in another clinical study within 3 months.
Study Design
Study Description
Connect with a study center
The Second Affiliated Hospital of Chongqing Medical University
Chongqing, Chongqing 4000000
ChinaActive - Recruiting
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