The Effect of Aromatherapy Applied After Cesarean Section on Pain Intensity and Comfort Level
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ClinicalTrials.gov Identifier: NCT06008964 |
Recruitment Status :
Completed
First Posted : August 24, 2023
Last Update Posted : October 26, 2023
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Condition or disease | Intervention/treatment | Phase |
---|---|---|
Cesarean Section Complications | Other: Ylang Ylang oil with inhalation Other: Lavender oil with inhalation | Not Applicable |
Study Type : | Interventional (Clinical Trial) |
Actual Enrollment : | 96 participants |
Allocation: | Randomized |
Intervention Model: | Parallel Assignment |
Masking: | Triple (Care Provider, Investigator, Outcomes Assessor) |
Primary Purpose: | Supportive Care |
Official Title: | Determination of the Effect of Aromatherapy Using Lavender and Ylang Ylang Essential Oils on Pain Severity and Comfort Level After Cesarean Section: A Randomized Controlled Study |
Actual Study Start Date : | June 15, 2023 |
Actual Primary Completion Date : | August 17, 2023 |
Actual Study Completion Date : | October 25, 2023 |
Arm | Intervention/treatment |
---|---|
Active Comparator: Ylang Ylang oil Group
GROUP 1
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Other: Ylang Ylang oil with inhalation
Ylang Ylang OIL WILL BE INHALED |
No Intervention: Control Group
No intervention
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Active Comparator: Lavender oil
GROUP 2
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Other: Lavender oil with inhalation
LAVENDER OIL WILL BE INHALED |
- pain related to cesarean section [ Time Frame: post operative 4-8-12 hours ]It will be measured with Visual Analog Scale. Visual Analog Scale has a rating between 0-10. The higher the score, the greater the pain.
- comfort related to cesarean section [ Time Frame: post operative 4-8-12 hours ]Comfort will be measured with the postpartum comfort scale. The higher the score, the higher the comfort level.
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Ages Eligible for Study: | 18 Years to 49 Years (Adult) |
Sexes Eligible for Study: | Female |
Gender Based Eligibility: | Yes |
Gender Eligibility Description: | Women aged 18-49 who have undergone cesarean section |
Accepts Healthy Volunteers: | Yes |
Inclusion Criteria:
- 18-49 years old,
- women who have had a cesarean section
Exclusion Criteria:
- epilepsy,
- migraine,
- chronic headache,
- asthma,
- women who are allergic to fragrance sensitivities to aromatic oils
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT06008964
Turkey | |
KTO Karatay University | |
Konya, Turkey, 42000 |
Study Chair: | şerife irem döner | serifeiremdoner@gmail.com | |
Study Chair: | Merve Yazar | merve.yazar@karatay.edu.tr |
Responsible Party: | Hafize Dağ Tüzmen, LECTURER, KTO Karatay University |
ClinicalTrials.gov Identifier: | NCT06008964 |
Other Study ID Numbers: |
Aromatherapy Group |
First Posted: | August 24, 2023 Key Record Dates |
Last Update Posted: | October 26, 2023 |
Last Verified: | October 2023 |
Individual Participant Data (IPD) Sharing Statement: | |
Plan to Share IPD: | No |
Studies a U.S. FDA-regulated Drug Product: | No |
Studies a U.S. FDA-regulated Device Product: | No |
Aromatherapy pain ceserean |