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

Completed · Phase 2

Conditions studied: Adenoid Hypertrophy

In brief

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.

Key facts

Study ID

NCT03714919

Run by

Arlyne Thung

People needed

10

Starts

2019-08-02

Expected to finish

2019-11-10

Last updated by the study team

2021-02-05

Who can join

Age: 4 and older, up to 8. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Patients undergoing adenoidectomy ± bilateral ear tube placement
• Have a parent/guardian who are compliant with routine medical care, capable of subjective evaluation and able to read, understand and sign the informed consent in accordance with IRB regulations

You may not qualify if…

• An American Society of Anesthesiologists Physical Status ≥ 4 (severe disease that is life threatening);
• A known hypersensitivity or allergy to any of the study medications;
• A history of chronic opioid use prior to surgery;
• Coexisting renal or hepatic disease;
• Morbid obesity (BMI% ≥ 99).

Where it is running

• Nationwide Children's Hospital — Columbus, Ohio, United States

Full record on ClinicalTrials.gov

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