Could a scent and a touch soothe Post-Surgery pain?
NCT ID NCT07743736
First seen Aug 04, 2026 · Last updated Sep 02, 2026 · Updated 3 times
Summary
This trial tests whether aromatherapy with rose oil or a massage using that oil can reduce pain, anxiety, and discomfort in women after a cesarean delivery. About 90 first-time mothers will be randomly assigned to receive one of these treatments or a placebo. The goal is to see if these gentle, non-drug approaches can improve well-being during early recovery.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Aromatherapy inhalation with Rosa damascena essential oil and aromatherapy-assisted back massage
- What this could lead to
- If effective, these simple, drug-free techniques could offer new ways to improve comfort and reduce pain and anxiety for women recovering from cesarean delivery.
- What could go wrong
- This is a small, early-stage trial, and the benefits may not be large or lasting. Individual responses to aromatherapy and massage can vary, and the placebo effect may play a role.
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
-
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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90 people
The number who actually took part.
- Started
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Feb 2026
- Finished
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Jul 2026
- 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 to 40 years
- Sex
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Female participants only
- 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.
Women aged 18-40 years Primiparous women Undergoing cesarean delivery under spinal anesthesia Term pregnancy (38-42 gestational weeks) Able to communicate and complete study questionnaires Willing to participate and provide written informed consent No known allergy to essential oils Intact sense of smell
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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.
Contacts and locations
Locations
-
Usak University Training and Research Hospital
Uşak, Uşak, 64200, Turkey (Türkiye)
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Other studies related to the condition(s) this trial covers.
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