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.
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…
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