The effect of topical application of lavender essential oil on physiological indexes and pain intensity during venous cannulation

The effect of topical application of lavender essential oil on physiological indexes and pain intensity during venous cannulation in patient whit were hospitalized in surgery unit

Status

Recruiting

Phases

Phase 3

Study type

Interventional

Source

IRCT

Registry ID

IRCT20171226038078N2

Enrollment

Registered

2018-02-24

Start date

2018-03-01

Completion date

Unknown

Last updated

2018-03-26

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

Conditions

Condition 1: Inguinal hernia. Condition 2: Gallstone. Inguinal hernia Disorders of gallbladder, biliary tract and pancreas in diseases classified elsewhere

Interventions

Intervention 1: In the intervention group, immediately prior to sedation, the amount of blood pressure, heart rate, Percentage of arterial oxygen saturation is measured and recorded. Then the lavender

Eligibility

Sex/Gender

All

Age

18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Patients who are Hospitalized for elective surgery Patients aged 18 to 65 years old The patient is completely alert The patient has the ability to communicate verbally The patient is not allergic to Iodine and Leukoplast adhesive There is a suitable vessel in the anterior region of the left hand

Exclusion criteria

Exclusion criteria: It is not possible to make a venous line at the desired location The patient used a sedative and anti-anxiety drug for at least 8-6 hours before referral A patient with Neuropathy, diabetes or other disease that affected on pain perception The patient has other pain and discomfort before the intravenous line Patient with psychological disorders based on medical records The patient is addicted

Design outcomes

Primary

Measure	Time frame
Pain severity score based on the visual scale of pain. Timepoint: Immediately after fixing the angiocate. Method of measurement: Visual Analogue Scale.;Heart rate. Timepoint: Before, immediately, 5 minutes and 10 minutes after completing the intravenous line. Method of measurement: the watch.;Blood Pressure. Timepoint: Before, immediately, 5 minutes and 10 minutes after completing the intravenous line. Method of measurement: Mercury barometric.;Percentage of arterial oxygen saturation. Timepoint: Before, immediately, 5 minutes and 10 minutes after completing the intravenous line. Method of measurement: Pulse oximeter.	—

Measure

Time frame

Pain severity score based on the visual scale of pain. Timepoint: Immediately after fixing the angiocate. Method of measurement: Visual Analogue Scale.;Heart rate. Timepoint: Before, immediately, 5 minutes and 10 minutes after completing the intravenous line. Method of measurement: the watch.;Blood Pressure. Timepoint: Before, immediately, 5 minutes and 10 minutes after completing the intravenous line. Method of measurement: Mercury barometric.;Percentage of arterial oxygen saturation. Timepoint: Before, immediately, 5 minutes and 10 minutes after completing the intravenous line. Method of measurement: Pulse oximeter.

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Countries

Iran (Islamic Republic of)

Contacts

Public ContactHasan Khalili

Sabzevar University of Medical Sciences

Khalili894@gmail.com+98 51 4401 8449

Outcome results

None listed

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