Effect of Aromatherapy on Perioperative Anxiety Level in Cesarean Sections
Anxiety, Midazolam Overdose, Breast Feeding

About this trial
This is an interventional supportive care trial for Anxiety focused on measuring aromatherapy, lavandula, sedative, spinal anesthesia, Anxiety
Eligibility Criteria
Inclusion Criteria:
- Pregnant women who underwent CS with spinal anesthesia
- Ninety-six patients aged between 18 and 45 years,
- With a height of ≥156 centimeters (cm)
- Gestational age of >37 weeks
- The American Society of Anesthesiologists (ASA) II risk group, who were scheduled for elective CS under spinal anesthesia
Exclusion Criteria:
-
Sites / Locations
- KahramanmarasSIU
Arms of the Study
Arm 1
Arm 2
Experimental
Placebo Comparator
the aromatherapy group
the control group
After the birth of the baby, two drops of 100% pure medical lavender oil (Lavandula angustifolia) was inhaled for 5 min through an oxygen mask by groups A and C, respectively. After 5 min, 2 mg intravenous midazolam for sedation was administred to the patients who gained 1 point from the Ramsey Sedation Scale (RSS). Complications, such as nausea, vomiting, hypotension (mean arterial pressure<60 mmHg), and allergies that developed after aromatherapy, were recorded. At the end of the operation, the dose added to the initial midazolam dose for all patients and the total surgical time were recorded. VAS pain and STAI-I scores were re-evaluated at the third postoperative hour, and the satisfaction levels of each patient after aromatherapy were recorded according to the Likert scale as "very satisfied, satisfied, moderate, and not at all satisfied".
Then, after the birth of the baby two drops of odorless baby oil (jojoba and almond oil) was inhaled for 5 min through an oxygen mask by groups A and C, respectively. After 5 min, 2 mg intravenous midazolam for sedation was administred to the patients who gained 1 point from the Ramsey Sedation Scale (RSS). Complications, such as nausea, vomiting, hypotension (mean arterial pressure<60 mmHg), and allergies that developed after aromatherapy, were recorded. At the end of the operation, the dose added to the initial midazolam dose for all patients and the total surgical time were recorded. VAS pain and STAI-I scores were re-evaluated at the third postoperative hour, and the satisfaction levels of each patient after aromatherapy were recorded according to the Likert scale as "very satisfied, satisfied, moderate, and not at all satisfied".