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COMPARISON OF THE EFFECTS OF ERECTOR SPINAE PLANE (ESP) BLOCK AND QUADRO İLİAC PLANE (QIP) BLOCK ON POSTOPERATIVE OPIOID CONSUMPTION AND PAIN IN LUMBAR SPINAL SURGERY

NCT07852104 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2026-09-01
Last updated
2026-10-01

Condition(s) studied

Postoperative Pain Management

Investigational drug(s) / intervention(s)

NRS Scoretotal tramadol consumptionPost Operative Pain Relievers →

NRS Score: An 11-point Numerical Rating Scale (NRS), where 0 indicated no pain and 10 represented the worst pain imaginable, was used to assess patients' pain levels.

total tramadol consumption: The total number of patient-controlled analgesia (PCA) bolus doses delivered within the first 24 hours will record

Post Operative Pain Relievers: All patients in the ward will be administered intravenous paracetamol every 8 hours, and intramuscular diclofenac sodium (75 mg) if the NRS score is 4 or higher.

Study summary

COMPARISON OF THE EFFECTS OF ERECTOR SPINAE PLANE (ESP) BLOCK AND QUADRO İLİAC PLANE (QIP) BLOCK ON POSTOPERATIVE OPIOID CONSUMPTION AND PAIN IN LUMBAR SPINAL SURGERY

Eligibility

Sex
ALL
Min age
18 Years
Max age
75 Years
Healthy volunteers
No
Inclusion Criteria: 1. Undergoing elective lumbar spinal surgery 2. ASA I-III 3. Aged 18-75 years Exclusion Criteria: - 1. Refusal at the time of enrollment 2. Request to withdraw from the study 3. Inability to provide informed consent 4. Emergency surgery 5. Bleeding diathesis 6. Presence of contraindications to the local anesthetic (LA) agents used in this study 7. Chronic opioid use 8. Psychiatric disorders 9. Presence of infection at the injection site

Primary outcome measure(s)

  • To compare the effects of the Quadro İliac Plane Block and the Erector Spinae Plane (ESP) Block on postoperative opioid consumption in lumbar spinal surgeries — 24 hour
    All patients will be administered tramadol via PCA, and the amount of tramadol consumed will be assessed at the end of the 24-hour postoperative period.

Trial sites (1)

FacilityCityRegionStatus
Aydin Adnan Menderes Üniversitesi Tip Fakültesi Hastanesi Aydin Turkey (Türkiye)
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07852104 on ClinicalTrials.gov ↗ ← All trials in Turkey