Infrared Thermography for Prediction of Successful Erector Spinae Plane Block in Unilateral Inguinal Hernia Surgery in Paediatric Patients

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age3-6
SponsorCairo University

About this trial

This study aims to evaluate the accuracy of temperature change (ΔT) measurements using infrared thermography to predict a successful erector spinae plane block in pediatric patients undergoing inguinal hernia repair under general anesthesia.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Age from 3 months to 6 years.

Both genders.

American Society of Anesthesiologists (ASA) Physical Status I-II.

Children undergoing elective unilateral open inguinal hernia surgery.

Disqualifiers

Parents' or guardians' refusal

Known Allergy to local anesthetics.

Coagulopathy [international normalised ratio (INR) >1.4 or platelets <75.000].

Infection at the site of injection or wound close to the puncture site.

Trial population

The study will be conducted at Kasr Al Ainy, Abu El Reesh children hospital.

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

  • Infrared Thermography

    Device

    Infrared thermography will be used to predict the success of an erector spinae block by measuring the temperature difference between the blocked and unblocked sides.

Treatment groups

69 Participants
are divided into 1 treatment group
Group A: Study group1 intervention

Trial outcomes

Primary outcomes

1

Predict successful ESPB

The ability to predict a successful erector spinae plane block by infrared thermography through the change in temperature (ΔT) (degrees Celsius) between the blocked and unblocked sides of the same dermatomal level in the mid-clavicular line throughout 20 minutes of block.

Time frame
Throughout 20 minutes of block

Secondary outcomes

1

Degree of pain

Degree of pain will be assessed using Face, Legs, Activity, Cry, and Consolability (FLACC) score. Each category is scored from 0 to 2, resulting in a total pain score from 0 to 10, where 0 indicates no pain and higher scores represent increasing pain levels. FLACC will be recorded at 15, 30, 45 and 60 min, 6 and 12 hours after surgery.

Time frame
12 hours after surgery
2

Heart rate

Heart rate will be recorded 5 min after intubation, then every 5 min after block 5,10,15, and 20 min, then at skin incision, immediately after extubation, 15 min after extubation, and every 15 minutes in the post-anesthesia care unit (PACU) (30,45, and 60 minutes) till discharge of the patient.

Time frame
Till discharge of the patient (Up to 12 hours)
3

Systolic blood pressure

Systolic blood pressure will be recorded 5 min after intubation, then every 5 min after block 5,10,15, and 20 min, then at skin incision, immediately after extubation, 15 min after extubation, and every 15 minutes in the post-anesthesia care unit (PACU) (30,45, and 60 minutes) till discharge of the patient.

Time frame
Till discharge of the patient (Up to 12 hours)
4

Mean arterial blood pressure

Mean arterial blood pressure will be recorded 5 min after intubation, then every 5 min after block 5,10,15, and 20 min, then at skin incision, immediately after extubation, 15 min after extubation, and every 15 minutes in the post-anesthesia care unit (PACU) (30,45, and 60 minutes) till discharge of the patient.

Time frame
Till discharge of the patient (Up to 12 hours)

Other outcomes

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