Erector Spinae Plane Block for Chronic Pain After Spinal Surgery

NCT ID
NCT07834502
Registry status
Not yet recruiting
Study type
Interventional
Phase
Not applicable
Sponsor
Aydin Adnan Menderes University
Conditions
Chronic Postsurgical Pain, Postoperative Pain, Spinal Surgery

Overview

ClinicalTrials.gov lists this study as Not yet recruiting.

Official title: Evaluation of the Effect of the Erector Spinae Plane (ESP) Block on Chronic Postoperative Pain After Lumbar Spine Surgery

Enrollment: 80 participants (Estimated).

What is being studied

  • Diagnostic test: BPI
  • Diagnostic test: NRS SCORE
  • Drug: Post Operative Pain Relievers
  • Diagnostic test: S-LANSS
  • Diagnostic test: Total tramadol consumption

Who may be eligible

Ages
18 Years to 75 Years
Sex
All
Healthy volunteers accepted
No

ClinicalTrials.gov lists the following eligibility criteria.

Inclusion Criteria: 1. Undergoing elective lumbar spinal surgery 2. ASA I-III 3. Aged 18-75 years Exclusion Criteria: Refusal to participate at the time of enrollment Request to withdraw from the study Inability to provide informed consent Emergency surgery Bleeding diathesis Presence of contraindications to the local anesthetic agents used in the study Chronic opioid use Psychiatric disorders Infection at the injection site

Study locations

1 study location is listed.

Site recruitment status is not specified in the registry data for these locations.

Countries: Turkey (Türkiye)

Sample of listed locations

  • AYDIN ADNAN MENDERES ÜNİVERSİTESİ TIP FAKÜLTESİ HASTANESİ, Aydın, 09100 — Aydin, 09100, Turkey (Türkiye) — Site recruitment status not specified in the registry data

Study details

Start date
October 1, 2026
Primary completion date
October 1, 2028
Completion date
January 1, 2029
First posted
September 22, 2026

Source and update information

Source
ClinicalTrials.gov
NCT ID
NCT07834502
Registry last updated
September 22, 2026
QualifiedStudies registry data refreshed
September 28, 2026
QualifiedStudies record fetched
September 28, 2026

View NCT07834502 on ClinicalTrials.gov

Trial information can change. Confirm current study details with the study team or the registry.

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