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

Infrared Thermography for Prediction of Successful Erector Spinae Plane Block in Unilateral Inguinal Hernia Surgery in Paediatric Patients: A Prospective Observational Study

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07161375
Enrollment
69
Registered
2025-09-08
Start date
2024-08-05
Completion date
2025-09-01
Last updated
2025-09-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Infrared, Thermography, Prediction, Erector Spinae Plane Block, Unilateral Inguinal Hernia Surgery, Paediatric

Brief summary

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.

Detailed description

Lower abdominal surgeries, including inguinal hernia repair, have been performed extensively in the daily practice of pediatric surgeries, so ensuring sufficient intra- and post-operative analgesia is crucial for perioperative care. The ultrasound-guided erector spinae plane block (ESPB) is a regional anesthetic technique. Early detection of successful ESPB in pediatric patients will enable the application of rescue techniques at the appropriate time, thereby improving patient satisfaction and reducing operating theatre time. There is considerable evidence regarding the value of infrared thermography in predicting successful nerve blocks. Infrared thermography is the process of using a thermal image to detect radiation (heat) coming from an object, converting it to temperature, and displaying an image of the temperature distribution.

Interventions

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.

Sponsors

Cairo University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
3 Months to 6 Years
Healthy volunteers
No

Inclusion criteria

* 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.

Exclusion criteria

* 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. * preexisting neuropathy (with sensory and/or motor deficits). * Diseases interfere with thermal imaging (as skin infections). * Baseline oesophageal body temperature of more than 37.5 °C. * Emergency and re-do cases will be excluded.

Design outcomes

Primary

MeasureTime frameDescription
Predict successful ESPBThroughout 20 minutes of blockThe 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.

Secondary

MeasureTime frameDescription
Heart rateTill discharge of the patient (Up to 12 hours)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.
Systolic blood pressureTill discharge of the patient (Up to 12 hours)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.
Degree of pain12 hours after surgeryDegree 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.
Number of doses of rescue analgesia12 hours after surgeryNumber of doses of rescue analgesia will be recorded.
Incidence of adverse events12 hours after surgeryIncidence of adverse events will be recorded.
Mean arterial blood pressureTill discharge of the patient (Up to 12 hours)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.

Countries

Egypt

Contacts

Primary ContactMarwa A Abdelfatah, Master
Marote7a@gmail.com00201065276941

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026