appendicitis. (K00-K93)
Conditions
Interventions
Intervention 1: Intervention group: In the aromatherapy group with geranium essence three grams of aromatic geranium essential oil of 1% maked by Barij Essence company are poured onto a pad and patien
Sponsors
Neyshabour University of Medical Sciences
Neyshabour University of Medical Sciences
Eligibility
Sex/Gender
All
Age
15 Years to 45 Years
Inclusion criteria
Inclusion criteria: Satisfied to participate in the study Appendectomy is undergoing open procedure Under general anesthesia After surgery, they are alert and have no known cognitive or psychological disorder Patients with anesthesia risks 1 and 2 The age of patients is between 15 and 45 years Do not consume drugs and not addicts Do not have a history of allergies and allergies There are no known underlying diseases Duration of surgery should not exceed one hour Do not have NG tube
Exclusion criteria
Exclusion criteria: The occurrence of any unexpected complications during an intervention that prevents further work with the patient, such as a severe reduce in blood pressure and other complications that may interfere with the patient's experience Deny the patient from participating in the intervention
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pain score according to VAS scale. Timepoint: Measuring the intensity of pain when entering the operating room, when the patient enters recovery in the first time that the patient is able to respond, when leaving the recovery, 4 hours after surgery. Method of measurement: VAS Scale.;Vomiting Nausea Score based on the visual scale of the severity of nausea. Timepoint: Before entering the operating room, after entering the recovery, immediately after the second intervention, before leaving the recovery, 4 hours after the operation. Method of measurement: the visual scale of the severity of nausea.;Physiological Indices. Timepoint: Before entering the operating room, before induction of anesthesia, before the operation, after the completion of the operation, after entering the recovery, immediately after the second intervention, before leaving the recovery. Method of measurement: Using finger pulse oximeter and monitoring device. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactMahnaz Abavisani
Neyshabour University of Medical Sciences
Outcome results
None listed