Post-surgical Pain Assessment in Children: Roles of Skin Conductance and Genomics

Pain Clinical Trial

Official title: Post-surgical Pain Assessment in Children: Roles of Skin Conductance and Genomics

Status Active, not recruiting

Clinical Trial Summary

Pain assessment in infants and toddlers is quite challenging since children in these populations are nonverbal or preverbal and cannot describe the presence and severity of pain that they perceive. Over the last decade, advances in the field have included the development of behavioral scoring systems for the assessment of acute pain . However, although they have been validated, these commonly used methods of pain assessment are largely subjective and rely on a highly trained observer. An objective continuous measure of pain would be an important addition to standard behavioral painscores which require nurses to monitor the child's behavioral responses.

Clinical Trial Description

After standard general anesthetic mask induction, 0.5 ml of blood will be drawn for genetic analysis when the intravenous catheter is sited. A member of the research team will manually transport an appropriately-labeled blood collection tube to the Department of Anesthesiology Perioperative Genomics Laboratory for storage and further preparation for genetic analysis. The samples will be stored until the investigators have enough to process. The results will be stored in a secure database. The surgical procedure, anesthesia technique, intraoperative analgesia treatment and initial postoperative analgesia treatment will be standardized.Upon arrival in the Post-Anesthesia Care Unit(PACU), the child will be connected to standard monitors as per standard of care. Pain scores will be recorded on a scale of 0-10 (FLACC, Face, legs,activity, cry, consolability scale) scale. A member of the research team will apply the skin conductance (SC) monitor on the child's hand or foot.This will be used to measure SC values that will be saved on a laptop computer and the SC data will be analyzed off-line. ;

Related Conditions & MeSH terms

• Pain
• Pain, Postoperative

• NCT number: NCT02534168
• Study type: Interventional
• Source: Milton S. Hershey Medical Center
• Status: Active, not recruiting
• Phase: N/A
• Start date: November 16, 2015
• Completion date: December 12, 2025