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Retrolaminar Block for Postoperative Analgesia in Lumbar Herniectomy Surgery

NCT04343937 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 30

Last updated 2020-09-21

No results posted yet for this study

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.

Conditions

  • Postoperative Pain

Interventions

PROCEDURE

retrolaminar block

local anesthetic injection on the between the lamina of the vertebra and the paraspinous muscle

Sponsors & Collaborators

  • Erzincan University

    lead OTHER

Eligibility

Min Age
18 Years
Max Age
70 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2020-04-15
Primary Completion
2020-06-15
Completion
2020-06-15

Countries

  • Turkey (Türkiye)

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04343937 on ClinicalTrials.gov