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Does melatonin after tonsillectomy enhance sleep and recovery in children (MATES)?

A multicentre, double blinded randomised controlled trial investigating the efficacy of postoperative Melatonin in improving children’s sleep quality and recovery post-tonsillectomy.

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12624000252516
Acronym
MATES
Enrollment
102
Registered
2024-03-14
Start date
2024-04-23
Completion date
2027-02-01
Last updated
2025-12-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Brief summary

Tonsillectomy is one of the most common childhood surgical procedures, however the postoperative recovery is often long and challenging for children and their families. This study aims to investigate if seven days of oral melatonin is able to improve sleep and pain management in children post-tonsillectomy, without increasing the risk of postoperative complications compared to placebo. We hypothesise that: (1) Melatonin will improve sleep following tonsillectomy; (2) melatonin will decrease post-operative pain and reduce breakthrough opioid requirement; and (3) melatonin will not increase the risk of post-operative complications.

Interventions

The study will be a randomized, double-blinded and placebo-controlled trial. Following approval from the treating anaesthetist and voluntary written informed consent by the parent/guardian, the recruited children will be block randomised and assigned to one of the two groups in a 1:1 ratio to receive either a melatonin solution or placebo solution. As part of the study development, the melatonin dosing was discussed with paediatric pain specialists, respiratory specialists and anaesthetists f

The study will be a randomized, double-blinded and placebo-controlled trial. Following approval from the treating anaesthetist and voluntary written informed consent by the parent/guardian, the recruited children will be block randomised and assigned to one of the two groups in a 1:1 ratio to receive either a melatonin solution or placebo solution. As part of the study development, the melatonin dosing was discussed with paediatric pain specialists, respiratory specialists and anaesthetists from Perth Children’s Hospital and other Australian centres. A conservative consensus dosing regime was agreed upon. Patients will receive their first dose 30-45 minutes prior to their usual bedtime on the day of surgery and continue on days 1-6 post-operatively (total of 7 doses). Children will receive a dose of 0.1 mg/kg (of ideal body weight) to a maximum of 5 mg of melatonin or placebo suspension at night by mouth for all their post operative doses. As a medical sleeping aid 1-10 mg is considered to be standard. Sedative premedications administered prior to surgery time (midazolam, clonidine, dexmedetomidine and ketamine) will be allowed as deemed appropriate by the treating anaesthetist. There will be active follow up with the families to ensure study adherence. All families are provided with a standard diary to document medication administration following tonsillectomy surgery. Our families will also be provided with a study diary where they will document further information. They will also report this in the study database via survey links sent daily.

Sponsors

Perth Children's Hospital
Lead SponsorHospital

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Treatment
Masking
Blinded (masking used) (Subject, Caregiver, Outcomes Assessor)

Eligibility

Sex/Gender
All
Age
2 Years to 16 Years
Healthy volunteers
No

Inclusion criteria

Children aged 2-16 years Undergoing elective surgery under general anaesthetic for tonsillectomy +/- adenoidectomy +/- grommets or cautery inferior turbinates Staying overnight in hospital

Exclusion criteria

• Currently taking Melatonin • Known cardiovascular, respiratory or neurological disorders giving an American Society of Anaesthesiologists (ASA) physical status classification III or above status • Known hypersensitivity to the active substance or to any of the excipients listed • Language barriers impeding data collection • Department for Child Protection and Family Support is involved in their care • Planned admissions to the Paediatric Intensive Care Unit (PICU) • Any concern in the ability of the parents/guardian or child to appropriately adhere to the study protocol or any issues which, in the investigator’s opinion, would increase the risks of study participation to the child. • Day surgery tonsillectomy

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026