Lavender oil massage may ease pain after lung surgery, new trial hopes
NCT ID NCT07622602
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tests whether applying a lavender oil blend to the skin around the surgical area can improve recovery quality after lung surgery. Researchers will compare the lavender oil to plain almond oil in 124 adults. The main goal is to see if aromatherapy helps reduce pain and improve overall recovery in the first few days after surgery.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- lavender essential oil diluted in sweet almond oil
- What this could lead to
- If it works, this could offer a simple, natural way to help people feel better and recover more comfortably after lung surgery.
- What could go wrong
- This is a small, early-stage trial. The effect may be small or no better than plain almond oil. Aromatherapy is not a substitute for standard pain care.
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 124 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Jun 2026
An estimate. Start dates often move.
- Expected to finish
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Jun 2028
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
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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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Adults aged 18 years or older, * undergoing scheduled lung resection for diagnostic or therapeutic purposes * able to give free, informed, signed consent (no later than the day of inclusion and before any examination required by the research) * person affiliated with or beneficiary of a social security system. Exclusion Criteria: * Patients with chronic pain prior to surgery * patients undergoing daily pain relief treatment prior to surgery * patients using essential oils applied to the skin for pain relief. * In relation to aromatherapy: * history of allergy to essential oils * atopic skin * known allergies * asthma * pregnant or breastfeeding women * nut allergies (in relation to sweet almond oil) * individuals who are vulnerable or deprived of their liberty by judicial or administrative decision * patients participating in other interventional studies on pain.
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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 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.
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