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Influence of Lavender Oil on Vital Signs in Oral Surgery Patients

NCT03722771 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 126

Last updated 2020-06-11

No results posted yet for this study

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.

Conditions

  • Dental Anxiety
  • Sedative; Anxiety Disorder

Interventions

BEHAVIORAL

Inhalation

lavender oil inhalation in a separate room for 3 minutes prior to surgery

OTHER

Anxiety Questionnaires 1

Modified Dental Anxiety Scale was used to describe the level of the dental anxiety.

OTHER

Anxiety Questionnaires 2

State-Trait Anxiety Inventory-State Scale was used to distinguish the true anxiety level of the patients from the anxiety level for a particular situation.

DIAGNOSTIC_TEST

Vital Signs 1

Changes in vital signs 1 - blood pressure - before, during and after the procedure were noted.

DIAGNOSTIC_TEST

Vital Signs 2

Changes in vital signs 2 - respiratory rate - before, during and after the procedure were noted.

DIAGNOSTIC_TEST

Vital Signs 3

Changes in vital signs 3 - heart rate - before, during and after the procedure were noted.

DIAGNOSTIC_TEST

Vital Signs 4

Changes in vital signs 4 - saturation - before, during and after the procedure were noted.

Sponsors & Collaborators

  • Nazife Begüm KARAN

    lead OTHER

Principal Investigators

  • Nazife Begüm KARAN · Recep Tayyip Erdogan University

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
37 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2017-09-01
Primary Completion
2018-11-02
Completion
2018-11-02

Countries

  • Turkey (Türkiye)

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03722771 on ClinicalTrials.gov