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Investigating The effect of peppermint oil on nausea, vomiting and post-operative pain in patients

Investigating The effect of peppermint oil on nausea, vomiting and post-operative pain in patients undergoing Rhinoplasty surgery: A Randomized Controlled Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20210927052608N2
Enrollment
64
Registered
2023-04-28
Start date
2023-05-27
Completion date
Unknown
Last updated
2023-05-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

patients undergoing Rhinoplasty surgery.

Interventions

Intervention 1: Intervention group: Peppermint essential oil... patients in the case group are prescribed 20 oral drops (2% peppermint essence) made by Alice company half an hour before surgery. Inter

Sponsors

Rasht University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Being at least 18 years old and at most 65 years old under elective rhinoplasty and septorhinoplasty surgery Not allergic to mint No smoking and drugs Patients should be in ASA class (I, II). Not breastfeeding

Exclusion criteria

Exclusion criteria: Failure to comply with the desired anesthesia protocol Receiving anti-nausea medication before or during anesthesia Reluctance to cooperate

Design outcomes

Primary

MeasureTime frame
Nausea. Timepoint: Recovery, ward, one hour after entering the ward. Method of measurement: Questionnaire of demographic information and to check vomiting through observation and evaluation of nausea based on nursing reports and patients' statements and also VAS scale for pain is used.;Recovery, ward, one hour after entering the ward. Timepoint: Recovery, ward, one hour after entering the ward. Method of measurement: Questionnaire of demographic information and to check vomiting through observation and evaluation of nausea based on nursing reports and patients' statements and also VAS scale for pain is used.

Secondary

MeasureTime frame
Pain. Timepoint: Recovery, ward, one hour after entering the ward. Method of measurement: VAS scale for pain.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactReza Pourmohammad

Rasht University of Medical Sciences

r_pourmohammad@yahoo.com+98 13 4366 4045

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026