Nausea. Nausea and vomiting
Conditions
Interventions
Intervention 1: In this study the researcher, after patients transferring from operating room to the surgical ward and stabilizing their vital signs performs the intervention between 2 groups. In the
Treatment - Other
Placebo
In this study the researcher, after patients transferring from operating room to the surgical ward and stabilizing their vital signs performs the intervention between 2 groups. In the first group that
In the control group, distilled water is used. two ml of distilled water were shed on the non Sterile gaz and the non sterile gaz is subjected to the patient's nose in a distance of 5 cm for 5 minutes
Sponsors
Kermanshah University of Medical Sciences
Eligibility
Sex/Gender
All
Age
15 Years to 65 Years
Inclusion criteria
Inclusion criteria: Inclusion criteria: Patients has been undergoing abdominal surgery; Having a good sense of smell(Ability to detect the scent of peppermint); Ages between 15 to 65 years; Having a good eyesight(to detect the severity of nausea on VAS); Having consciousness; Not suffering from asthma and other allergic diseases; Non-smoking; Receiving a type of anesthesia(general); Receiving a group of drug during anesthesia(Nesdonal and Isoflurane). Exclusion Criteria: Patient with lack of cooperation during the study; Loss of consciousness; Receiving Antiemetic drugs; Receiving narcotic drug(Morphine and Pethidine)during the study.
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Nuasea severity. Timepoint: Before the intervention, 5 and 10 minutes after intervention. Method of measurement: Visual Analog Scale to assessment of nausea. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactYasin Ahmadi
Kermanshah University of Medical Sciences
Outcome results
None listed