Impact of Topical Aromatherapy on Postoperative Quality of Recovery After Lung Resection
- Sponsor
- University Hospital, Toulouse
- Study ID
- NCT07622602
- Status
- Not Yet Recruiting
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Conditions
- Aromatherapy
- Complementary Therapies
- Pain
- Postoperative Recovery
- Thoracic Surgical Procedures
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- topical application of the "AromaQoR" formulation — OTHERtopical application of the "AromaQoR" formulation, containing lavender essential oil (Lavandula angustifolia) diluted to 5% in sweet almond vegetable oil around the operated area
- topical application of sweet almond vegetable oil — OTHERtopical application of sweet almond oil around the operated area
Study Details
The key to early surgery recovery lies in optimal and immediate control of postoperative pain. Despite standard pain management protocols, lung resection is often associated with acute, neuropathic, or chronic pain, compounded by the side effects of morphine-based treatments. In this context, aromatherapy can provide complementary support, both to alleviate pain and to improve the quality of recovery after surgery.
Key Dates
- First listed
- Jun 3, 2026
- Start date
- Jun 30, 2026
- Status verified
- May 2026
- Primary completion
- Jun 30, 2028
- Completion
- Jun 30, 2028
Study Design
- Enrollment
- 124 participants (estimated)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- PREVENTION
Arms
- Placebo Comparator: PL =placeboThe PL group: In addition to standard pain relief treatments, the PL group will receive topical application of sweet almond oil around the operated area at 9 p.m. from day 0 to day 2.
- Experimental: AT = aromatherapyThe AT group: in addition to standard analgesic treatments, the AT group will receive topical application of the "AromaQoR" formulation, containing lavender essential oil (Lavandula angustifolia) diluted to 5% in sweet almond vegetable oil around the operated area at 9 p.m. from day 0 to day 2.
Primary Outcome Measure
Change in the total QoR-15F [ Time Frame: day 2 ]
Central Contacts
- claudia Lavedan5 67 77 18 74
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