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Lumbar Erector Spinae Plane Block in Knee Prosthesis

NCT04544423 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 34

Last updated 2020-09-10

No results posted yet for this study

Summary

To determine the postoperative analgesic efficiency of ultrasound-guided lumbar erector spinae plane block, patients are divided into two groups. Study group received ultrasound-guided lumbar erector spinae plane block, where control had none. Visual analog scale and opioid consumption are recorded.

Conditions

  • Block

Interventions

OTHER

Block group

Patients received lumbar erector spinae plane Block before operation

Sponsors & Collaborators

  • Tokat Gaziosmanpasa University

    lead OTHER

Principal Investigators

  • Hakan Tapar · Gaziosmanpasa University

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2020-09-02
Primary Completion
2021-09-02
Completion
2021-09-02

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 NCT04544423 on ClinicalTrials.gov