MedPath

Pediatric Delirium

Phase 4
Suspended
Conditions
Pediatric Delirium
Interventions
Registration Number
NCT04669457
Lead Sponsor
University of Massachusetts, Worcester
Brief Summary

Preventing emergent delirium in pediatric ambulatory surgery through preoperative use of intra-nasal Dexmedetomidine and oral Midazolam.

Detailed Description

Pediatric ambulatory patients will randomly be allocated to one of two groups. Group A which will receive Dexmedetomidine intra-nasally at a dose of 1 mcg/kg, approximately 15-25 minutes before entering the operating room or Group B which will receive Midazolam orally at a dose of 0.5 mg/kg (with a maximum dose of 20 mg), approximately 10-15 minutes before entering the operating room. Each subject will receive a Drug Acceptance scale, and Parental Separation Anxiety Scale (PSAS) mask Acceptance Scale to identify the differences in markers associated with pediatric delirium. End tidal Sevoflurane value during the surgery and at the time when patient leaves the OR, amount and dose of oral/rectal acetaminophen given in PACU, child's behavior for 48 hours post-operatively, and documented intake of oral analgesics will be collected to identify the reduced need for post-operative analgesia and behaviors associated with extended pediatric delirium.

Recruitment & Eligibility

Status
SUSPENDED
Sex
All
Target Recruitment
60
Inclusion Criteria
  • Subjects age 3 months to 9 years
  • Scheduled to undergo a myringotomy
  • American Society of Anesthesiologists (ASA) classification of I - II.
Exclusion Criteria
  • Subjects with unrepaired cardiac defects, including cyanotic congenital heart disease.
  • Anyone age 10 years or older.
  • Anyone with an ASA classification of III or higher.
  • Non-English language speaker for whom short form consent is not available.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Intra-nasal DexmedetomidineIntra-nasal DexmedetomidineSubjects will receive Dexmedetomidine intra-nasally in the preoperative area. It will be administered at a dose of 1 mcg/kg, approximately 15-25 minutes before entering the operating room.
Oral MidazolamOral MidazolamSubjects will receive Midazolam orally in the preoperative area. It will be administered at a dose of 0.5 mg/kg (with a maximum dose of 20 mg), approximately 10-15 minutes before entering the operating room.
Primary Outcome Measures
NameTimeMethod
Time to onset of pediatric deliriumZero minutes to 48 hours

Time from when the patient is woken from anesthesia to the onset of delirium.

Time to offset of pediatric deliriumZero minutes to 48 hours

Time from onset of delirium to the offset of delirium.

Duration of pediatric deliriumZero minutes to 48 hours

Total time patient experiences delirium

Secondary Outcome Measures
NameTimeMethod
Drug Acceptance10-25 minutes prior to surgery

The willingness of the subject to take the drug was assessed in the pre-operative area

Parental Separation Anxiety Scale (PSAS)0-48 hours

Anxiety score was determined when the child was separated from the parents according to four levels.

Mask Acceptance Scale1-10 minutes prior to surgery

The child's acceptance of the mask by the anesthesiologist was rated as follows.

End tidal Sevoflurane value0-12 hours

During the surgery and at the time when patient leaves the OR End tidal Sevoflurane value will be documented.

Rescue analgesia in PACU0-6 hours post surgery

The amount and dose of oral/rectal acetaminophen given in PACU was recorded.

Home Behavior Analysis12-48 hours

The child's parents were given a diary to document their behavior for 48 hours post-operatively at home.

Oral analgesic useTwo days post-operative

Document intake of oral analgesics like acetaminophen or ibuprofen

Trial Locations

Locations (1)

University of Massachusetts Medical School

🇺🇸

Worcester, Massachusetts, United States

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