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Clinical Trials/NCT02434731
NCT02434731
Completed
Phase 3

Randomized Controlled Trial to Evaluate the Effectiveness of Vibration and External Cold (Buzzy Device) for Pain Relief During Venipuncture or Intravenous Cannulation in Children With Intellectual Disability.

IRCCS Burlo Garofolo1 site in 1 country71 target enrollmentApril 2015
ConditionsPain Relief

Overview

Phase
Phase 3
Intervention
Not specified
Conditions
Pain Relief
Sponsor
IRCCS Burlo Garofolo
Enrollment
71
Locations
1
Primary Endpoint
Pain score (NCCPC-PV scale)
Status
Completed
Last Updated
10 years ago

Overview

Brief Summary

Needle procedures are the most common and important source of pain and distress in children in the health care setting. Children with intellectual disability from any cause experience pain more frequently than healthy children. They often require venipuncture or IV cannulation for diagnostic or therapeutic procedures. Pain in this population is often unrecognised because these patients are frequently unable to self-report their pain. Now it's possible to measure pain in children with intellectual disability with specific pain scales, like NCCPC-PV (Non-Communicating Children's Pain Checklist, Post-operative Version).

The efficacy of a device combining vibration and cold for pain relief during venipuncture or IV cannulation has been recently reported in children. The device's actions are based on the Gate Control Theory, whereby cold and vibrations stimulate large fiber and inhibitory neurons to interrupt nociception. This non-pharmacologic technique for pain relief could be useful in this kind of patients in emergency department. To date, there is no study that validated Buzzy device for pain relief in children with intellectual disability.

The aim of this study is to test the effectiveness of Buzzy® (a device that provides cold and vibration), in reducing the pain during venipuncture or IV cannulation, in children with intellectual disability.

Registry
clinicaltrials.gov
Start Date
April 2015
End Date
June 2015
Last Updated
10 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
IRCCS Burlo Garofolo
Responsible Party
Principal Investigator
Principal Investigator

Ronfani Luca

MD, PhD

IRCCS Burlo Garofolo

Eligibility Criteria

Inclusion Criteria

  • Age 4 to 17 years
  • Presence of intellectual disability
  • Need of peripheral IV line or venipuncture
  • Informed consent signed by parents or legal guardians

Exclusion Criteria

  • Presence of abrasion, infection or break in skin in the area of Buzzy® placement
  • Cold hypersensibility

Outcomes

Primary Outcomes

Pain score (NCCPC-PV scale)

Time Frame: intraoperative

The pain during the procedure will be evaluated using the NCCPC-PV scale (Non-communicating Children's Pain Checklist - Postoperative Version) administered by a nurse

Secondary Outcomes

  • Number of attempts required(intraoperative)
  • Success at first attempt(intraoperative)
  • Adverse events(up to 15 minutes after the procedure)

Study Sites (1)

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