Dexmedetomidine as Adjuvant for Suprazygomatic Maxillary Nerve Block in Children's Adenotonsillectomy
Launched by MCGILL UNIVERSITY HEALTH CENTRE/RESEARCH INSTITUTE OF THE MCGILL UNIVERSITY HEALTH CENTRE · Jun 2, 2025
Trial Information
Current as of August 22, 2025
Not yet recruiting
Keywords
ClinConnect Summary
This clinical trial is studying the use of a medication called dexmedetomidine to help manage pain in children who are having a specific surgery called adenotonsillectomy, which involves removing the tonsils and adenoids. The researchers want to see if using dexmedetomidine alongside a local anesthetic (ropivacaine) can lead to less pain after surgery and improve how well the children recover at home without needing opioids, which are strong pain medications.
To be eligible for the trial, children must be scheduled for this type of surgery and show signs of significant sleep-related breathing issues. Parents must speak either French or English to participate. During the study, children will receive the nerve block during surgery and will be monitored afterward for their pain levels, how much pain medication they need, and their overall recovery. They will also answer questions about their pain and recovery for a week after the surgery. This trial is not yet recruiting participants, but it aims to help improve pain management strategies for children undergoing this common procedure.
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • Scheduled for elective partial adenotonsillectomy,
- • STUBR score ≥ 3, indicating significant sleep-disordered breathing
- • Patients whose parents are fluent in French of English will be enrolled
- Exclusion Criteria:
- • Scheduled to undergo total extracapsular adenotonsillectomy or adenoidectomy-only procedures
- • Patient requires prolonged intubation postoperatively
- • the anesthesiologist does not adhere to the standardized anesthesia protocol
- • Patients with neurological or cardiac congenital deficits, with cardiac arrhythmias (non-sinus rhythm), implanted pacemakers, on chronic therapy with drugs that have known effects on sympathetic and parasympathetic activity (antimuscarinics, beta-2 adrenergic agonists, alpha-1 adrenergic antagonists or antiarrhythmic agents, tricyclic antidepressants)
- • ASA physical status III or higher
- • Parent/legal guardians refuses to participate
- • Patients scheduled for surgery without an appointment at the Montreal Children's Hospital (MCH) Preoperative Clinic will not be enrolled in the study.
About Mcgill University Health Centre/Research Institute Of The Mcgill University Health Centre
The McGill University Health Centre (MUHC) and the Research Institute of the McGill University Health Centre (RI-MUHC) are leading institutions in clinical research and healthcare innovation. With a commitment to advancing medical knowledge and improving patient outcomes, the MUHC integrates cutting-edge research with high-quality patient care. The RI-MUHC fosters a collaborative environment where multidisciplinary teams engage in transformative research across various fields, including oncology, neurology, and cardiovascular health. By leveraging state-of-the-art facilities and a robust network of clinical expertise, both entities strive to translate scientific discoveries into effective treatments, ultimately enhancing the quality of life for patients locally and globally.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Montreal, Quebec, Canada
Patients applied
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported