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Clinical Trials/NCT03722771
NCT03722771
Completed
Not Applicable

Influence of Lavender Oil on Vital Signs and Anxiety in Oral Surgery Patients: a Randomized Controlled Clinical Trial

Nazife Begüm KARAN1 site in 1 country126 target enrollmentSeptember 1, 2017

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Dental Anxiety
Sponsor
Nazife Begüm KARAN
Enrollment
126
Locations
1
Primary Endpoint
Vital Sign Measurements - 1 - changes in blood pressure
Status
Completed
Last Updated
5 years ago

Overview

Brief Summary

The aim of this study is to investigate the impact of lavender oil (Lavandula angustifolia) on anxiety, mood, vital signs (blood pressure, respiratory rate, heart rate and saturation) for oral surgery patients.

Detailed Description

Lavender oil has sedative properties. Oral surgical procedures have been proven as to be the greatest concern among dental practices for patients. Limited randomized clinical trials have demonstrated evidence-based results of lavender oil, despite being the most effective essential oil for anxiety and stress. The hypothesis of the present study was that the inhalation of lavender oil prior to oral surgical procedures may reduce anxiety and consequently may effect intra and post-operative blood pressure, inspiration and heart rate.

Registry
clinicaltrials.gov
Start Date
September 1, 2017
End Date
November 2, 2018
Last Updated
5 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Nazife Begüm KARAN
Responsible Party
Sponsor Investigator
Principal Investigator

Nazife Begüm KARAN

Assistant Professor, DDS, PhD

Recep Tayyip Erdogan University Training and Research Hospital

Eligibility Criteria

Inclusion Criteria

  • Clinical diagnosis of wisdom tooth
  • Must be similar in age-height-weight
  • Must be similar socio-culturally

Exclusion Criteria

  • Under 18 years of age
  • Taking psychotropic medication or psychiatric treatment
  • Systemically unhealthy patients
  • Pregnants

Outcomes

Primary Outcomes

Vital Sign Measurements - 1 - changes in blood pressure

Time Frame: through study completion an average of 3 months

changes in blood pressure

Vital Sign Measurements - 2 - changes in respiratory rate

Time Frame: through study completion an average of 3 months

changes in respiratory rate

Vital Sign Measurements - 4 - changes in saturation level

Time Frame: through study completion an average of 3 months

changes in saturation level

Vital Sign Measurements - 3 - changes in heart rate

Time Frame: through study completion an average of 3 months

changes in heart rate

Secondary Outcomes

  • Anxiety Test 2 - STAI-S tests(through study completion an average of 3 months)
  • Anxiety Test 1 - MDAS tests(through study completion an average of 3 months)

Study Sites (1)

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