Effects of Aromatic Solution Applied After Surgery
Surgery, Nurse's Role, Throat, Sore
About this trial
This is an interventional prevention trial for Surgery focused on measuring surgical nursing, complementary alternative medicine, non-pharmacological applications, post-operative care, aromatherapy, sore throat, thirst, nausea vomiting
Eligibility Criteria
Inclusion Criteria:
- Accepting the research
- Elective surgery planned with general anesthesia
- Patients in Asa I, II and III classes
- No hearing problem
- No history of allergies to lavender and ginger
- One-time intubation and no difficult intubation
- Those who have no previous psychiatric or mental illness will be included.
Exclusion Criteria:
- Did not accept the research
- In addition to clinical routine medical treatment, extra drug administration
- Patients with suspected aspiration risk will be excluded.
Sites / Locations
- Cukurova University
Arms of the Study
Arm 1
Arm 2
Arm 3
Experimental
Placebo Comparator
No Intervention
Experimental group (group treated with aromatic solution)
Placebo group (group treated with drinking water)
Control Group
Informed consent form will be signed by the patients selected by randomization and a personal information form will be filled. Hour 0: The patients will be completely awakened from the anesthesia resting unit, their vital signs will be stable, they will be transferred to the clinic where they lie normally with a 15 glaskow scale, the bed head will be elevated 45 degrees and the risk of aspiration will be ruled out. After controlling the vital signs of the patient, sore throat and thirst with VAS and nausea and vomiting with the verbal descriptive scale VDS will be evaluated. After the data are collected, the aromatic solution will be shaken and applied to the oral cavity and throat as a spray 4 times. After the aromatic solution application is finished, the patients' sore throat, thirst and nausea and vomiting will be re-evaluated with the same forms. 2., 4., 6. The same procedures will be repeated in the 8th and 8th hours.
Patients included in this group as a result of randomization will have to sign an informed consent form and fill out a personal information form. Hour 0: The patients will be completely awakened from the anesthesia resting unit, their vital signs will be stable, they will be transferred to the clinic where they sleep normally with a 15 glaskow scale, the bed head will be elevated 45 degrees and the risk of aspiration will be ruled out. Nausea and vomiting will be evaluated with a verbal descriptive scale. After the data are collected, drinking water will be applied to the oral cavity and throat in the form of a spray 4 times. After the drinking water application is finished, the patients' sore throat, thirst and nausea and vomiting will be re-evaluated with the same forms. 2., 4., 6. The same procedures will be repeated in the 8th and 8th hours.
Patients in the control group were planned to be followed according to their clinical procedures. Since there were no procedures or interventions in the clinical procedures, it was decided to follow up only the patient, and the control group patients to be followed up at the same times with the same forms. Patients included in this group as a result of randomization will have to sign an informed consent form and fill out a personal information form. Hour 0: Patients will be transferred from the recovery unit to the clinic. After controlling the vital signs of the patient, sore throat and thirst with VAS and nausea and vomiting with a verbal descriptive scale will be evaluated. 2., 4., 6. The same procedures will be repeated in the 8th and 8th hours.