Menu
Recruiting NCT07161375

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

Observational Infrared Thermography Prediction Erector Spinae Plane Block

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Infrared Thermography.
Who it may be relevant to
Registry conditions: Infrared, Thermography, Prediction, Erector Spinae Plane Block. Basic parameters: 3 months — 6 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Egypt
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

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

Overview

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

  • Device Infrared Thermography
    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.

Primary outcome measures

  • Predict successful ESPB [Time frame: Throughout 20 minutes of block]
Secondary outcome measures (6)
  • Degree of pain [Time frame: 12 hours after surgery]
  • Heart rate [Time frame: Till discharge of the patient (Up to 12 hours)]
  • Systolic blood pressure [Time frame: Till discharge of the patient (Up to 12 hours)]
  • Mean arterial blood pressure [Time frame: Till discharge of the patient (Up to 12 hours)]
  • Number of doses of rescue analgesia [Time frame: 12 hours after surgery]
  • Incidence of adverse events [Time frame: 12 hours after surgery]

Eligibility criteria

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.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Cohort

Study locations

Egypt · 1 center
  • Cairo University — Cairo

Identifiers

NCT: NCT07161375 · MD-210-2024

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗