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Retrolaminar Block for Postoperative Analgesia in Lumbar Herniectomy Surgery

Postoperative Pain Clinical Trial

Official title:
Retrolaminar Block for Postoperative Analgesia in Lumbar Herniectomy Surgery

Clinical Trial Summary

This retrospective study included 30 patients scheduled for lumbar herniectomy under general anesthesia. The patients were randomized to receive either retrolaminar block or intravenous analgesia treatment.Numeric Pain Rating Scale (NPRS) was used to measure the pain intensity of patients in postoperative period. Postoperative analgesic requirements were recorded to asses effectiveness of regional anesthesia.Opiod and NSAİD as rescue medication were recorded postoperatively.

Clinical Trial Description

This retrospective study included 30 patients scheduled for lumbar herniectomy under general anesthesia. The patients were randomized to receive either RLB or intravenous analgesia treatment. All patients were routinely monitored and their heart rate, blood pressure and pulse oxymetry recorded during the anesthesia. Numeric Pain Rating Scale (NPRS) scores evaluated at 2, 8, 12, 24 and 48 h after the surgery. Opiod and NSAİD as rescue medication were recorded postoperatively ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04343937
Study type Observational
Source Erzincan University
Contact
Status Completed
Phase
Start date April 15, 2020
Completion date June 15, 2020
View Details
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