Clinical TrialID 7932
The Effect of Aromatherapy Applied After Cesarean Section on Pain Intensity and Comfort Level
NCT06008964
Cesarean Section Complications
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Record Fields
Scalar fields from the final clinical_trial record.
- Clinical Trial Id
- 7932
- Evidence Id
- 7932
- Core Evidence Id
- 7932
- Source Clinical Trial Id
- 7928
- Herb2 Clinical Trial Id
- HBCT007928
- Nct Id
- NCT06008964
- Title
- The Effect of Aromatherapy Applied After Cesarean Section on Pain Intensity and Comfort Level
- Status
- Completed
- Phase
- Study Result
- No
- Study Condition
- Cesarean Section Complications
- Study Type
- Interventional
- Study Design
- Allocation: RANDOMIZED|Intervention Model: PARALLEL|Masking: TRIPLE (CARE_PROVIDER, INVESTIGATOR, OUTCOMES_ASSESSOR)|Primary Purpose: SUPPORTIVE_CARE
- Intervention
- OTHER: Ylang Ylang oil with inhalation|OTHER: Lavender oil with inhalation
- Intervention Allocation
- Randomized
- Intervention Model
- Parallel
- Intervention Mask
- Triple
- Intervention Purpose
- Supportive_Care
- Gender
- Female
- Age
- Adult
- Enrollment
- 96
- Outcome Measure
- pain related to cesarean section, 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., post operative 4-8-12 hours
- Sponsor Collaborator
- KTO Karatay University|Şerife İrem DÖNER|Merve YAZAR|JULE ERİÇ HORASANLI
- Funded By
- OTHER
- Location
- KTO Karatay University, Konya, 42000, Turkey
- Other Id
- Aromatherapy Group
- Start Date
- 2023-06-15
- Primary Completion Date
- 2023-08-17
- Completion Date
- 2023-10-25
- First Posted
- 2023-08-24
- Results First Posted
- Last Update Posted
- 2023-10-26
- Study Document
- Study Url
- https://clinicaltrials.gov/study/NCT06008964
- Title Cn
- Title En
- The Effect of Aromatherapy Applied After Cesarean Section on Pain Intensity and Comfort Level
- Bilingual Status
- semi_complete