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Clinical Trial Summary

Assess the efficacy and safety of the topic use of an eutectic mixture of local anesthetics for postoperative pain control of patients submitted to hemorrhoidectomy. Patients will be operated and discharged at the same day in a day hospital clinic. During the fourteen days recovery period, they will apply the study medication to the anal region 4 times daily. The Visual Analog Pain Scale (VAS) will be answered twice daily. Patients will also take 100 mg oral nimesulide twice daily and 50 mg tramadol on demand up to 4 times daily. The tramadol demand will be tabulated. A rescue medication for analgesia will be provided (sodium diclofenac IM).


Clinical Trial Description

n/a


Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT00932542
Study type Interventional
Source Federal University of São Paulo
Contact
Status Active, not recruiting
Phase Phase 2/Phase 3
Start date April 2010
Completion date November 2012

See also
  Status Clinical Trial Phase
Enrolling by invitation NCT06403774 - Bowel Preparation Before Hemorrhoidectomy N/A
Recruiting NCT04361695 - Preemptive Analgesia for Hemorrhoidectomy N/A
Recruiting NCT04288349 - IntraopeRativE Use of periNeal Block for Hemorrhoidectomy N/A
Completed NCT03938714 - Hemorrhoidectomy in Patients With Grade III and IV Disease:Harmonic Scalpel Compared With Conventional Technique N/A
Completed NCT03848468 - Comparison Study: Ligasure Versus Conventional Hemorrhoidectomy in III and IV Degree Hemorrhoids. N/A