Lumbar ESPB in Hip Replacement Surgery

NARecruitingINTERVENTIONAL
Enrollment

60

Participants

Timeline

Start Date

February 19, 2024

Primary Completion Date

February 1, 2025

Study Completion Date

August 1, 2025

Conditions
CoxarthrosisPain, PostoperativePain, AcutePain, ChronicPostoperative Pain, ChronicAnalgesiaQuality of LifeAnesthesiaSpinal
Interventions
PROCEDURE

Spinal anesthesia

Before the beginning of surgery, all patients will be anesthetized with 0.5 % hyperbaric bupivacaine (Marcaine Heavy), 1.5 - 2.5 mL solution. A pencil point spinal needle will be used.

PROCEDURE

lumbar erector spinae plane block

Investigators will perform the lumbar ESPB under ultrasound control at the L3 level on the ipsilateral site of the surgery. After dissection with 0.9 NaCl, we will leave a catheter in the ESP. Then, we used 0.25% bupivacaine with epinephrine (5mcg/mL), 0.4 mL per kg, up to 40 mL.

PROCEDURE

Epidural analgesia

After identifying the epidural space and spinal anesthesia (combined technique), a catheter will be placed in the epidural space. Investigators will give an epidural catheter a test dose of 2% lidocaine (2 mL). At the end of the surgery, the patient will receive 5 mL of a mixture containing 0.1% bupivacaine with fentanyl (2 mcg/mL).

PROCEDURE

patient-controlled analgesia

Each participant will receive a pump with oxycodone (1mg/ml) using a patient-controlled analgesia (PCA) technique, a bolus of 1 mL, and a lockout of 5 minutes for the first postoperative day.

DIAGNOSTIC_TEST

Timed Up and Go test

Investigators will measure the time the patient took to rise from a chair, walk three meters, turn around 180 degrees, walk back to the chair, and sit down while rotating 180 degrees. We will assess the patient before the surgery and 24 and 48 hours after hip replacement.

DIAGNOSTIC_TEST

neuropathic pain symptom inventory

The Neuropathic Pain Symptom Inventory (0-100; 0 denotes no pain, 100 the most severe pain) will be evaluated before the surgery and three and six months following the procedure.

DIAGNOSTIC_TEST

Lovett test

A physiotherapist will use the six-grade Lovett scale to measure muscle strength, in which 0 denotes no muscle contractility, and 5 denotes the complete range of motion against gravity, with full resistance. We will test this before the surgery, 24 and 48 hours after the operation.

DIAGNOSTIC_TEST

Visual analog scale

Investigators will measure pain intensity with VAS (0-10; 0 denotes no pain, 10 maximal pain) before and after the surgery. Pain will be evaluated at rest and upon the activity.

DIAGNOSTIC_TEST

Quality of Recovery 40

Investigators will assess the quality of recovery with QoR-40 a day after the surgery, a month, and three months following the procedure. The minimal score is 40, and the maximal is 200. The higher the result, the better the quality of recovery is.

DIAGNOSTIC_TEST

Ability to sit, stand upright, and walk

A physiotherapist will evaluate the patient's ability to sit, stand upright, and walk at planned times.

Trial Locations (1)

20-081

RECRUITING

II Department of Anesthesia and Intensive Care, Lublin

All Listed Sponsors
lead

Medical University of Lublin

OTHER