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Clinical Trials/NCT03330496
NCT03330496
Completed
Not Applicable

Using Machine-learning Algorithms to Assess Acute Pain in Nonverbal Infants

Stanford University1 site in 1 country43 target enrollmentOctober 30, 2017
ConditionsPain, Acute

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Pain, Acute
Sponsor
Stanford University
Enrollment
43
Locations
1
Primary Endpoint
Pain Measurement (all infants)
Status
Completed
Last Updated
3 years ago

Overview

Brief Summary

Pain assessments in non-verbal, critically ill infants represent an important clinical challenge. Older children or adults can easily express their pain, but infants lack that capability. They frequently experience repetitive acute pain during routine ICU care, but their analgesic management flounders on the horns of a dilemma: (a) failure to treat infant pain leads to immediate clinical instability and potentially long-term physical, behavioral, and cognitive sequelae, vs. (b) strong analgesics may increase risks for medical complications and/or impaired brain growth. Bedside nurses currently assess pain using pain scores, before taking action to ameliorate pain. Pain scores increase nursing workload and provide subjective assessments, rather than objective data for evaluating infant pain. Consequently, infants exposed to skin-breaking procedures, surgery, or other painful conditions often receive variable and inconsistent pain management in the ICU. The investigators aim to develop a multimodal pain assessment system, using sensor fusion and novel machine learning algorithms to provide an objective measure of pain that is context-dependent and rater-independent. This will enhance the quality of pain management in ICUs and allow continuous pain monitoring in real-time.

Registry
clinicaltrials.gov
Start Date
October 30, 2017
End Date
March 30, 2022
Last Updated
3 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Kanwaljeet Anand

Professor of Pediatrics, Anesthesiology, Perioperative & Pain Medicine

Stanford University

Eligibility Criteria

Inclusion Criteria

  • All infants less than 6 months of corrected chronological age.
  • Infants admitted to the participating ICUs at LPCH (NICU, PICU, CVICU).
  • Require an acute painful procedure for routine clinical care.

Exclusion Criteria

  • Newborns with birth trauma, intrapartum asphyxia (5-minute Apgar Score \<4 or cord pH \< 7.01), fetal growth restriction (birth weight \< 5th percentile for gestation), congenital anomalies or metabolic disorders, or any kind of brain injury.
  • Newborns born to mothers with a history of heavy smoking or drug abuse (alcohol, cocaine, ketamine, heroin/other opiates) or psychiatric drugs used during this pregnancy.
  • Newborns and infants requiring positive pressure ventilation using a face mask (BiPAP) or endotracheal tube (conventional or high-frequency ventilators).
  • Newborns and infants receiving continuous infusions of opioid drugs (morphine, fentanyl, others) and nerve blocks or neuraxial analgesia affecting the site of the invasive procedure during the 24 hours prior to study entry. (Note: Infants receiving intermittent opioids or non-opioid analgesics (acetaminophen, ibuprofen, ketorolac, others) WILL NOT be excluded).
  • Newborns and infants with facial anomalies, injuries or other pathologies affecting the facial area.

Outcomes

Primary Outcomes

Pain Measurement (all infants)

Time Frame: 10 minutes

Visual Analogue Scale (VAS) measures pain intensity based on observer assessment on a scale from 1 to 10, where higher values indicate more intense pain.

Secondary Outcomes

  • Pain Measurement (newborns 0-30 days)(8 minutes)
  • Pain Measurement(30 minutes)
  • Pain Measurement (infants 1-6 months)(3 minutes)

Study Sites (1)

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