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A Pilot Study: a Non-opioid Technique for Postoperative Adenoidectomy Pain Relief in Pediatric Patients

NCT03714919 · Status: COMPLETED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 10

Last updated 2021-02-05

Study results available
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Summary

This proposed study will assess analgesic efficacy of a multi-modal, non-opioid analgesic regimen for providing surgical analgesia in pediatric patients undergoing adenoidectomy and to assess recovery characteristics in the post-anesthesia care unit (PACU) and at home following surgery.

Conditions

  • Adenoid Hypertrophy

Interventions

DRUG

Dextromethorphan

Preoperative oral dextromethorphan 1 mg/kg

DRUG

Acetaminophen

Preoperative oral acetaminophen 15 mg/kg

DRUG

Dexmedetomidine

Intraoperative intravenous dexmedetomidine 0.5 μg/kg

DRUG

Ketamine

Intraoperative intravenous ketamine 0.5 mg/kg

Sponsors & Collaborators

  • Arlyne Thung

    lead OTHER

Principal Investigators

  • Arlyne Thung, MD · Nationwide Children's Hospital

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
4 Years
Max Age
8 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-08-02
Primary Completion
2019-11-10
Completion
2019-11-10
FDA Drug
Yes

Countries

  • United States

Study Locations

More Related Trials

Entities

Drugs

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03714919 on ClinicalTrials.gov