Could a spoonful of honey ease Post-Surgery pain?
NCT ID NCT06275698
First seen Jul 07, 2026 · Last updated Jul 08, 2026 · Updated 1 time
Summary
This study investigates whether Manuka honey can help reduce pain after tonsillectomy (surgery to remove the tonsils). Adults undergoing the procedure will take either honey or a placebo syrup three times daily for 14 days, alongside standard pain medication. The goal is to see if honey improves pain control and recovery, offering a simple, low-cost alternative to conventional painkillers.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Manuka honey
- What this could lead to
- If it works, this could offer a low-cost, natural option to help manage pain after tonsillectomy, potentially reducing the need for painkillers.
- What could go wrong
- This is a small, early-stage trial, and previous evidence is mixed. The honey may not prove more effective than placebo, and some people may have allergies or dislike the taste.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 100 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Sep 2023
- Expected to finish
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Jul 2027
An estimate. End dates often move.
- Lead sponsor
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A government agency
The lead sponsor is a government body.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Adult (≥18years old at the time of giving consent) * Consented and listed for bilateral tonsillectomy or adenotonsillectomy * Tonsillectomy performed within the trial study period Exclusion Criteria: * Any concurrent Head \& Neck (H\&N) malignancy * Unilateral tonsillectomy * Pregnancy * Concurrent pharyngeal or upper aerodigestive tract biopsy * Robotic tonsillectomy * Previous H\&N malignancy * Previous H\&N radiotherapy * Type 1/2 diabetes mellitus * Known allergy to bee related products * Known allergy to golden syrup * History of chronic pain * History of fibromyalgia * Current usage of chronic (\>6weeks) analgesia * High-risk anaesthetic patients * Children or adolescents \<18years old * Adults unable to consent for themselves
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Lister Hospital
RECRUITINGStevenage, SG1 4AB, United Kingdom
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