Clinical Trials Directory

Trials / Completed

CompletedNCT04343937

Retrolaminar Block for Postoperative Analgesia in Lumbar Herniectomy Surgery

Status
Completed
Phase
Study type
Observational
Enrollment
30 (actual)
Sponsor
Erzincan University · Academic / Other
Sex
All
Age
18 Years – 70 Years
Healthy volunteers
Not accepted

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.

Detailed 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

Conditions

Interventions

TypeNameDescription
PROCEDUREretrolaminar blocklocal anesthetic injection on the between the lamina of the vertebra and the paraspinous muscle

Timeline

Start date
2020-04-15
Primary completion
2020-06-15
Completion
2020-06-15
First posted
2020-04-14
Last updated
2020-09-21

Locations

1 site across 1 country: Turkey (Türkiye)

Source: ClinicalTrials.gov record NCT04343937. Inclusion in this directory is not an endorsement.