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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

ConditionPostoperative Pain Management
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-75
SponsorAydin Adnan Menderes University

About this trial

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 criteria

This trial does not accept healthy volunteers

Qualifiers

Undergoing elective lumbar spinal surgery

ASA I-III

Aged 18-75 years

Disqualifiers

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

Trial design

Design model

Parallel

Treatments tested in this trial

  • NRS Score

    Diagnostic test

    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

    Diagnostic test

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

  • Post Operative Pain Relievers

    Drug

    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.

Treatment groups

80 Participants
are divided into 2 treatment groups
Group A: ESP BLOCKActive comparator 3 interventions
Group B: QIP BLOCKExperimental treatment 3 interventions

Trial outcomes

Primary outcomes

1

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

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.

Time frame
24 hour

Secondary outcomes

1

To compare the effects of the Quadro iliac (Qıp) block and the Erector Spinae Plane (ESP) block on postoperative pain in lumbar spinal surgeries

The NRS score will be assessed on a scale of 0 to 10, with 0 representing the lowest and 10 the highest value; patients will be asked to provide a rating at the 12th hour.

Time frame
12th hour

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Aydin Adnan Menderes University

Lead sponsor

Source ClinicalTrials.gov

This trial is not recruiting at the moment. You can still explore other options: