Effect of Patient Position on Erector Spinae Plane Block in Thoracic Surgery

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-75
SponsorDr Abdurrahman Yurtaslan Ankara Oncology Training and Research Hospital

About this trial

The erector spinae plane (ESP) block is a widely used regional anesthesia technique for postoperative analgesia in thoracic surgery. The block can be performed in different patient positions, most commonly sitting or lateral decubitus, but the effect of patient position on dermatomal sensory spread and analgesic efficacy has not been clearly established.

This prospective, randomized, single-blind clinical trial aims to compare the effects of ESP block performed in sitting versus lateral decubitus position on dermatomal sensory distribution and postoperative analgesic outcomes in patients undergoing video-assisted thoracic surgery.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Age 18 to 75 years

ASA physical status II-IV

Scheduled for elective video-assisted thoracic surgery

Ability to provide written informed consent

Disqualifiers

Known allergy to local anesthetics

Chronic opioid use

Preexisting chronic pain

Severe cognitive impairment

Trial design

Design model

Parallel

Treatments tested in this trial

  • Erector Spinae (ESP) Block with Bupivacaine (Marcaine®) sitting position

    Drug

    Erector spinae plane block-sitting position

  • Erector Spinae (ESP) Block with Bupivacaine (Marcaine®) lateral position

    Drug

    Erector Spinae Plane Block-Lateral position

Treatment groups

90 Participants
are divided into 2 treatment groups
Group A: Sitting Position GroupActive comparator 1 intervention
Group B: Lateral Decubitus Position GroupExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Dermatomal sensory spread

Cranial and caudal sensory limits and total number of dermatomes affected, assessed by cold sensation and pin-prick testing.

Time frame
15 minutes after the block application

Secondary outcomes

1

Postoperative pain scores (Numeric Rating Scale)

Numeric Rating Scale, 0-10 points, 0=no pain, 10= worst pain imaginable

Time frame
Postoperative 0, 2, 6, 12, and 24 hours
2

Total opioid consumption

Time frame
First 24 postoperative hours

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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

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