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Clinical Trial Summary

The purpose of this study is to compare the quality and duration of pain relief after a hemorrhoidectomy, provided by locally administered liposomal bupivacaine versus bupivacaine hcl or control with saline. It is hypothesized that liposomal bupivacaine will provide more effective postoperative pain relief than both bupivacaine hcl and the control.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02104414
Study type Interventional
Source St. Luke's-Roosevelt Hospital Center
Contact
Status Terminated
Phase Phase 4
Start date April 2014
Completion date January 2016

See also
  Status Clinical Trial Phase
Enrolling by invitation NCT02353156 - Posthemorrhoidectomy Pain Management With Electronic Bidet or Sitz Bath Phase 2
Not yet recruiting NCT05089500 - The Two Treatment Methods Compared the Sclerosing Agent Injection and the Rubber Wrapping N/A
Completed NCT00890721 - Study of Pain Control in Hemorrhoidectomy Phase 3
Completed NCT01169311 - Safety and Performance of the Covidien EEA Hemorrhoid and Prolapse Stapling Set in a Hemorrhoidopexy Procedure N/A
Completed NCT01927874 - Subarachnoid or Infiltration for Hemorrhoidectomy N/A
Completed NCT01880775 - Discharge Conditions of Spinal Anesthesia With Heavy Prilocaine-Fentanyl and Heavy Bupivacaine-Fentanyl Phase 4