Clinical Trials Directory

Trials / Completed

CompletedNCT03460145

Lavender Oil on Preoperative Anxiety and Sedation Requirement in General Anaesthesia

Lavender Aromatherapy; Its Effect on Preoperative Anxiety and Propofol Requirement for Anaesthesia.

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
108 (actual)
Sponsor
Universiti Kebangsaan Malaysia Medical Centre · Academic / Other
Sex
Female
Age
18 Years – 65 Years
Healthy volunteers
Accepted

Summary

Assessment of how Lavender oil reduces preoperative anxiety and subsequently influences requirement of induction agents for general anesthesia.

Detailed description

This study aims to use aromatherapy (Lavender oil) to reduce Preoperative Anxiety among Female patients coming for elective surgeries under General Anesthesia. As a consequence of that, the effect is also evaluated on how that influences the amount of intravenous sedation is required during induction for General Anesthesia.

Conditions

Interventions

TypeNameDescription
OTHERLavender Oil on Nasal Strip (Lx)Usage of Aromatherapy for Preoperative Anxiety
OTHERStrip without Lavender Oil (Px)Strip without Lavender Oil (Px)
DRUGPropofol 1 % Injectable SuspensionPropofol 1% (10mg/mL)

Timeline

Start date
2018-09-27
Primary completion
2018-12-10
Completion
2019-01-01
First posted
2018-03-09
Last updated
2019-05-21

Locations

1 site across 1 country: Malaysia

Source: ClinicalTrials.gov record NCT03460145. Inclusion in this directory is not an endorsement.