- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04693390
Acupuncture in Emergency Delirium After Tonsillectomy
Acupuncture Management of Emergence Agitation in Children Undergoing Tonsillectomy: a Randomized Controlled Trial
Emergence delirium (ED) (also called emergence agitation) can be defined as a "dissociated state of consciousness in which the child is irritable, uncompromising, uncooperative, incoherent and inconsolable crying, moaning, kicking or thrashing".
Tonsillectomy (with or without adenoidectomy) is a routinely performed operation. Emergence agitation is a frequent phenomenon in children recovering from general anesthesia for tonsillectomy, and increases risk of self-injury. It's not unusual for the post-anesthesia care unit (PACU) staff look that a child, who was asleep just minutes before, starts screaming, pulling out his intravenous line, looks like he's about to fall out of his bed. This condition requires sedatives that may cause undesirable side effects. The cause of emergence delirium and the mechanism of agitation following general anesthesia is unknown. Probably the volatile agents work on some pathways, possibly in the locus coeruleus or amygdala, in the setting of a specific neurodevelopmental stage of the brain.
While emergence delirium can be seen into adulthood, its peak incidence is in younger children (2-7 years of age). The incidence of ED is unclear: anywhere from 2-80%, but when confounders like pain, nausea etc. are controlled, the incidence is probably around 20-30%.
Limited data suggest that acupuncture may be a safe, nonpharmacological treatment for the reduction of pain and agitation in term and preterm infants and that may be an alternative method for preventing ED. In particular a prospective, randomized, double-bind controlled study demonstrated a reduction of the ED in many surgeries, after the electrical stimulation of the heart 7 acupuncture site.
Nearly 400 acupuncture points are known on the body surface and they belong to 14 meridians, running along the human body. After the needle peeling, the nervous free terminations release some polypeptid (the most important is the substantia P) and it increases the excitability of the near nervous free terminations which cause vasodilatation. It has a myorelaxant effect, decreases the level for pain tolerance and make stronger the inhibitor effect of descendent fibers, with production of endogenous endorphins. This is the reason why acupuncture is considered valid in prevention and control of ED.
Study Overview
Study Type
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Silvia Tisato, MD
- Phone Number: 00390403785111
- Email: silvia.tisato@burlo.trieste.it
Study Contact Backup
- Name: Silvia Tisato, MD
- Phone Number: 00390403785111
- Email: siliva.tisato@burlo.trieste.it
Study Locations
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-
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Trieste, Italy, 34137
- Institute for Maternal and Child Health - IRCCS "Burlo Garofolo"
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion criteria
- Children scheduled to undergo tonsillectomy with or without adenoidectomy
- American Society of Anesthesiologist (ASA) physical status I or II
Exclusion criteria
- Coagulation disorders (pro-hemorrhagic status)
- Neurological disorders (development delay)
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Acupuncture
The acupuncture will be applied at points LI4, ST36, HT7, in association with auriculotherapy point Master Cerebral, immediately after induction of anesthesia for 20 minutes
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Application of acupuncture
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No Intervention: Standard care group
The patients will follow the standard procedure
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Postoperative agitation evaluated with the PAED scale
Time Frame: Within 5 minutes from arrival in the post anesthesia care unit
|
Between groups difference in postoperative agitation assessed by the health personnel with the Pediatric Anesthesia Emergence Delirium (PAED) scale.
PAED consists of 5 psychometric items describing emergence behavior, with score ranging from 0 to 20.
The severity of ED increases with a higher score.
Scores ≥10 indicate the presence of ED.
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Within 5 minutes from arrival in the post anesthesia care unit
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Postoperative agitation evaluated with the PAED scale
Time Frame: 30 minutes after the arrival in the post anesthesia care unit
|
Between groups difference in postoperative agitation assessed by the health personnel with PAED scale.
PAED consists of 5 psychometric items describing emergence behavior, with score ranging from 0 to 20.
The severity of ED increases with a higher score.
Scores ≥10 indicate the presence of ED.
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30 minutes after the arrival in the post anesthesia care unit
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Postoperative agitation evaluated with the Watcha Scale
Time Frame: Within 5 minutes from arrival in the post anesthesia care unit
|
Between groups difference in postoperative agitation assessed with the Watcha Scale.
The Watcha scale is a 4 points scale, describing the behaviour of the patient; a score >2 indicates emergence delirium.
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Within 5 minutes from arrival in the post anesthesia care unit
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Postoperative agitation evaluated with the Cravero scale
Time Frame: Within 5 minutes from arrival in the post anesthesia care unit
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Between groups difference in postoperative agitation assessed with the Cravero emergence agitation scale, consisting of five steps from obtunded and unresponsive to wild thrashing behaviour requiring restraint.
A score of 4 (from crying and difficult to console to wild thrashing) for 5 or more minutes is indicative of emergency delirium.
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Within 5 minutes from arrival in the post anesthesia care unit
|
Postoperative agitation evaluated with the Watcha Scale
Time Frame: 30 minutes after the arrival in the post anesthesia care unit
|
Between groups difference in postoperative agitation assessed with the Watcha Scale.
The Watcha scale is a 4 points scale, describing the behaviour of the patient; a score >2 indicates emergence delirium.
|
30 minutes after the arrival in the post anesthesia care unit
|
Postoperative agitation evaluated with the Cravero scale
Time Frame: 30 minutes after the arrival in the post anesthesia care unit
|
Between groups difference in postoperative agitation assessed with the Cravero emergence agitation scale, consisting of five steps from obtunded and unresponsive to wild thrashing behaviour requiring restraint.
A score of 4 (from crying and difficult to console to wild thrashing) for 5 or more minutes is indicative of emergency delirium.
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30 minutes after the arrival in the post anesthesia care unit
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Pain evaluated with the FLACC scale
Time Frame: Within 5 minutes from arrival in the post anesthesia care unit
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Between groups difference in pain, evaluated using the Faces, Legs, Activity, Cry and Consolability (FLACC) scale administered by the health personnel.
The FLACC tool assesses changes in five categories of behavior (namely: Face, legs, Activity, Crying and Consolability), rating each one on a scale of 0-2.
Ten is the maximum score indicating severe pain and a score <2 generally indicates absence of pain.
A FLACC score higher than 4 is considered as indicator of moderate pain.
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Within 5 minutes from arrival in the post anesthesia care unit
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Pain evaluated with the FLACC scale
Time Frame: 30 minutes after the arrival in the post anesthesia care unit
|
Between groups difference in pain, evaluated using the FLACC scale administered by the health personnel.
The FLACC tool assesses changes in five categories of behavior (namely: Face, legs, Activity, Crying and Consolability), rating each one on a scale of 0-2.
Ten is the maximum score indicating severe pain and a score <2 generally indicates absence of pain.
A FLACC score higher than 4 is considered as indicator of moderate pain.
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30 minutes after the arrival in the post anesthesia care unit
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Unintended harm caused by patients agitation
Time Frame: Within 5 minutes from arrival in the post anesthesia care unit
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Between groups difference in harming surgical repair, harming self or caregivers, pulling out IV's draws or tubes
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Within 5 minutes from arrival in the post anesthesia care unit
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Unintended harm caused by patients agitation
Time Frame: 30 minutes after the arrival in the post anesthesia care unit
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Between groups difference in harming surgical repair, harming self or caregivers, pulling out IV's draws or tubes
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30 minutes after the arrival in the post anesthesia care unit
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Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Silvia Tisato, MD, Institute for Maternal and Child Health IRCCS Burlo Garofolo
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- RC 33/2020
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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