Skip to main content
Clinical Trials/NCT03931343
NCT03931343
Unknown
N/A

Randomized, Double Blind Trial of Thoracolumbar Interfascial Plane Block and Erector Spinae Plane Block for Adult Spinal Surgery

Bezmialem Vakif University0 sites60 target enrollmentDecember 2020

Overview

Phase
N/A
Intervention
Not specified
Conditions
Postoperative Pain
Sponsor
Bezmialem Vakif University
Enrollment
60
Primary Endpoint
Total morphine consumption
Last Updated
5 years ago

Overview

Brief Summary

Spinal surgery is typically associated with severe postoperative pain. Although the number of spinal surgeries has increased day by day, postoperative pain management have been limited. The recently described thoracolumbar interfacial plane block (TLIPB) has been reported to provide effective postoperative analgesia in spinal surgery. In addition, the recently described erector spinae plane block (ESPB) is obtained by applying the local anesthetic drug between the fascia of the spina muscles and the transverse process of the vertebrae. Anatomical and radiological investigations in fresh cadavers suggest that the potential place of influence of ESPB is dorsal and ventral spinal nerve roots. A small number of publications showing the analgesic efficacy of ESP in spinal surgery have been reported in the literature. In this study, the investigators aimed to compare the analgesic efficacy of TLIPB and ESPB in spinal surgeries.

Registry
clinicaltrials.gov
Start Date
December 2020
End Date
April 2021
Last Updated
5 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Serdar Yeşiltaş

İnstructor

Bezmialem Vakif University

Eligibility Criteria

Inclusion Criteria

  • 20-75 years
  • Patients scheduled for elective surgery

Exclusion Criteria

  • Patients with previous neurological disease symptoms (TIA, syncope, dementia, etc.)
  • Allergy to drugs
  • Major cardiac disease
  • Renal failure
  • Psychiatric disease
  • Patients who refuse to participate in the study
  • Chronic back and lower back pain

Outcomes

Primary Outcomes

Total morphine consumption

Time Frame: 48 hour

The total amount of morphine given by patient controlled analgesia in 48 hours will be recorded.

Secondary Outcomes

  • Pain intensity score at rest(48 hour)
  • Pain intensity score at movement(48 hour)
  • Time to first rescue analgesia(48 hour)
  • Postoperative nausea and vomiting(48 hour)
  • Patient satisfaction score(48 hour)

Similar Trials