SPI-directed Analgesia for Lumbar Discectomy

• Status: Completed
• Trial end date: 2017-07-30
• Target enrollment: 0
• Participant gender: All

Summary

The aim of this randomized trial is to assess the efficacy of analgesia for lumbar discectomy and compare Numerical Rating Scale (NRS) with Surgical Pleth Index (SPI) for monitoring pain perception postoperatively.

Patients received either preemptive local tissue infiltration at surgical site using either 0,2% ropivacaine with fentanyl or 0,2% bupivacaine with fenthanyl or preemptive intravenous infusion using metamizole and tramadol.

• Phase: N/A
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Medical University of Silesia
• Collaborator: Silesian University of Medicine
• Treatments: Analgesics; Anesthetics; Anesthetics, Local; Bupivacaine; Dipyrone; Pharmaceutical Solutions; Ropivacaine; Tramadol

Criteria

Inclusion Criteria:

• written consent to participate in the study

• written consent to undergo general anaesthesia with local wound infiltration and surgery of discectomy

Exclusion Criteria:

• allergy to local anaesthetics

• necessity of administration of vasoactive drugs influencing SPI monitoring

• pregnancy