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Lavender Aromatherapy Spine Procedure Study

NCT04156009 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 109

Last updated 2021-02-02

No results posted yet for this study

Summary

Patient anxiety prior to invasive procedures poses a significant barrier to successful treatment if not well-managed. The purpose of this study is to evaluate lavender aromatherapy, a non-sedating alternative, to reduce anxiety prior to interventional spinal procedures.

Conditions

  • Spine Injuries and Disorders
  • Pain, Back

Interventions

OTHER

Activated Lavender Elequil aromatabs® (#372)

Activated Lavender aromatherapy tablets wrapped in tape

OTHER

Unactivated Lavender Elequil aromatabs® (#372)

Unactivated Lavender aromatherapy tablets wrapped in tape

Sponsors & Collaborators

  • Weill Medical College of Cornell University

    lead OTHER

Principal Investigators

  • Jaspal R Singh, MD · Weill Medical College of Cornell University

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
85 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2020-01-29
Primary Completion
2020-11-18
Completion
2020-11-18

Countries

  • United States

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 NCT04156009 on ClinicalTrials.gov