Overview

Opioid-Free Anesthetic for Tonsillectomy

Status:
Recruiting
Trial end date:
2023-12-31
Target enrollment:
0
Participant gender:
All
Summary
Prospective randomized controlled trial to determine if opioid-free anesthetic for tonsillectomy is non-inferior to standard opioid-containing anesthetic
Phase:
Phase 4
Accepts Healthy Volunteers?
Accepts Healthy Volunteers
Details
Lead Sponsor:
Children's Hospital of Philadelphia
Collaborators:
University of Pennsylvania
University of Tennessee Health Science Center
Treatments:
Dexmedetomidine
Fentanyl
Ketorolac
Morphine
Criteria
Inclusion Criteria:

1. Males or females age 2 to 18 years.

2. American Society of Anesthesiologists {ASA) ≤ 3 physical classification system

3. Girls after menarche must have a negative pregnancy test.

4. Scheduled tonsillectomy or tonsillectomy combined with adenoidectomy and/or ear tube
placement at the Children's Hospital of Philadelphia (CHOP) main or ambulatory
surgical centers.

5. Parental/guardian permission (informed consent) and if appropriate, child assent

Exclusion Criteria:

1. Current (Within the last 30 days) opioid use for pain control

2. High risk for surgical site hemorrhage, determined by bleeding disorder diagnosis or
evidence or poor hemostasis

3. Multiple scheduled surgeries at the same time other than adenoidectomy and/or ear tube
placement

4. History of drug abuse, chronic pain, bleeding disorder

5. Chronic disease such as sickle cell disease for which treatment with opioids may be
clinically indicated

6. Significant congenital disorders, medication allergies or comorbidities, specifically
a pre-disposition to bradycardia or conduction abnormalities, cyanotic cardiac disease
and use of medications that would increase risk of bleeding or bradycardia.

7. History of hepatic dysfunction, renal dysfunction, thrombocytopenia, or anemia
(including pre-surgery laboratory abnormalities)

8. History of hypersensitivity to NSAIDs

9. Patients with asthma, including patients who have experienced aspirin- or
NSAID-sensitive asthma or a history of exacerbation when aspirin or NSAIDs are
administered (e.g. bronchospasm, urticaria, etc.)

10. Subjects receiving medications that could impact metabolism of either study drug
should also be excluded

11. Trisomy 21 diagnosis

12. Parents/guardians or subjects who, in the opinion of the Investigator, may be
non-compliant with study schedules or procedures.

13. Patients on a Ketogenic diet

14. Parents or subjects who do not speak English