The Efficacy and Safety of Liposomal Bupivacaine in Relieving Postoperative Pain After Hemorrhoid Surgery

Recruiting N/A Interventional Study
Hemorrhoid Surgery Liposome Bupivacaine Pain Management Local Infiltration
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 – 64
Sex
Any
Study type
Interventional
Purpose
Treatment
Participants needed
156 (estimated)
Sponsor
Beijing Tiantan Hospital · Other
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About This Trial
Hemorrhoids represents the most prevalent condition among anorectal disorders. Due to the unique anatomical characteristics of the perianal region, patients frequently experience severe postoperative pain, which may lead some individuals to delay treatment due to pain-related anxiety. Consequently, effective postoperative pain management is critical for the recovery of hemorrhoid patients. Develop…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: 1. Patients scheduled for elective Hemorrhoid Surgery under general anesthesia; 2. Ages 18 to 64 years old; 3. American Society of Anesthesiologists (ASA) physical status of I-III; 4. Glasgow Coma Scale (GCS) score of 15; 5. Patients must be able to understand the nature and pot…
Contacts

Fang Luo

+86 13611326978

13611326978@163.com

CONTACT