Effect of Lavender Aromatherapy on Post-Operative Nausea and Vomiting Among Laparotomy Patients
Postoperative Nausea and Vomiting
About this trial
This is an interventional treatment trial for Postoperative Nausea and Vomiting
Eligibility Criteria
Inclusion Criteria: Patients from the age of 18 -65 years according to the ethical principles of world medical association (WMA) declaration of Helsinki Patients with both gender Male and Female Patients who will be administered general anesthesia for laparotomy Those who experience nausea and vomiting within 24hr following the laparotomy Patients who will be clinically stable Exclusion Criteria: • Patients who move to intensive care unit after surgery Patients with history of any type of addiction Patients with history of pre-op nausea and vomiting due to hospital environment Patients with history of motion sickness Patients who start Oral /NG Feed after laparotomy Patients with respiratory diseases, allergies, infections Reversal laparotomy within short duration Who received pre or intra-op antiemetic Those who experience any complication during laparotomy will be excluded from this study.
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Experimental
No Intervention
Intervention Group
Control group
After deciding on the participant of the intervention group the researcher will start the protocol of intervention The researcher will soak a 4×4 cm sterile gauze pad with 0.2 ml equivalent to 2 drops of 10% Lavender essential oil and will suspend the soaked gauze at a distance of 10cm from the patient's nose with the help of forceps, and he or she will have asked to inhale its scent for 5 min. 15 and 40 minutes after the beginning of the aromatherapy treatment, the researcher will measure the nausea and vomiting scores by using the standardized tool. During this entire 40 minutes, the researcher will strictly monitor the participant's condition. If the nausea score is still higher than 1 or the vomiting persists the participants will be noted as failure of treatment and move to standard care.
The control group received standard care against the complain of nausea and vomiting.