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NCT04260399 · ClinicalTrials.gov registry record · NA
Anxiety Reduction During Office Procedural Medicine Using Aromatherapy
A NA study, sponsored by Loyola University.
- Completed
- Registry status
- NA
- Development phase
- 88
- Enrollment target
NCT04260399 is a NA study that has completed, run by Loyola University. The registered enrollment target is 88 participants.
The verdict
NCT04260399, a NA study, has completed, sponsored by Loyola University.
- COMPLETED
- Registry status
- NA
- Development phase
- 88 participants
- Enrollment target
Study Summary
This goal of this study is to assess whether lavender aromatherapy during gynecologic and urogynecologic outpatient procedures is associated with a decrease in patient anxiety levels. Based on similar interventions in other specialties of medicine, the investigators hypothesize that patients exposed to lavender aromatherapy during their procedure will have less anxiety than those who are not exposed to lavender aromatherapy.
Interventions
- OTHER Lavender Aromatherapy
- OTHER Placebo Aromatherapy
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 88 participants |
| Start Date | 2020-02-18 |
| Est. Completion | 2021-05-26 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT04260399
The ClinicalTrials.gov registry entry for NCT04260399 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 88 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Loyola University, which has 92 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which Lavender Aromatherapy is the first listed.
NCT04260399 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT04260399 about?
NCT04260399 is a clinical study titled "Anxiety Reduction During Office Procedural Medicine Using Aromatherapy". This goal of this study is to assess whether lavender aromatherapy during gynecologic and urogynecologic outpatient procedures is associated with a decrease in patient anxiety levels. Based on similar interventions in other specialties of medicine, the investigators hypothesize that patients exposed...
What is the current status of trial NCT04260399?
This trial is currently completed. It is a NA study. The enrollment target is 88 participants. The study started on 2020-02-18. Estimated completion is 2021-05-26.
What interventions are being tested in trial NCT04260399?
The interventions under investigation include: Lavender Aromatherapy (OTHER), Placebo Aromatherapy (OTHER).
Who is sponsoring clinical trial NCT04260399?
This trial is sponsored by Loyola University, which has 92 total clinical trials registered on ClinicalTrials.gov.
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