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Clinical Trials/NCT02592044
NCT02592044CompletedPhase 4

Evaluation of the Effect of Aromatherapy With Lavender Essential Oil on Pain and Anxiety During Peripheral Venous Cannulation

Tokat Gaziosmanpasa University2 sites in 1 country106 target enrollmentStarted: November 1, 2015Last updated:
Conditions

Trial Snapshot

Phase
Phase 4
Status
Completed
Sponsor
Enrollment
106
Locations
2
Primary Endpoint
Pain Level

Study Overview

Brief Summary

The effect of aromatherapy with lavender essential oil on pain and anxiety during venipuncture will be evaluated.

Detailed Description

The anxiety and pain during venipuncture may be cause to the avoidance of the medical therapy in patient as well as adult. Aromatherapy with lavender was shown that beneficial effects on chronic pain and anxiety. It's effect on acute pain and anxiety is not exactly known. In this study, the aromatherapy with the lavender will be compared with placebo to evaluate the analgesic and anxiolytic effect during peripheral venous cannulation before surgery.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Single (Outcomes Assessor)

Eligibility Criteria

Ages
18 Years to 65 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • be scheduled for elective surgery
  • be accepted to inhale lavender

Exclusion Criteria

  • age <18 years >65 years
  • preoperative pain or consumption of analgesic medication
  • anxiety disorders or consumption of anxiolytic medications (i.e. SSRI, benzodiazepine)
  • pregnancy or breastfeeding
  • asthma, chronic obstructive pulmonary disease
  • poor sense of smell
  • allergy to the lavender essential oil

Outcomes

Primary Outcomes

Pain Level

Time Frame: Within the first 5 minutes after the peripheral venous cannula insertion process

The pain of the patients during cannulation will be measured with Visual Analog Scale from 0 to 10.

Secondary Outcomes

  • Anxiety Level(Within the first 5 minutes after the peripheral venous cannula insertion process)
  • Patient Satisfaction(Within the first 15 minutes after the peripheral venous cannula insertion process)

Investigators

Sponsor
Tokat Gaziosmanpasa University
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Tuğba Karaman

Assistant Professor

Tokat Gaziosmanpasa University

Study Sites (2)

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