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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03130218
Other study ID # 2016-74-LGH
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date June 8, 2017
Est. completion date December 31, 2019

Study information

Verified date February 2020
Source Lancaster General Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Determine the effectiveness of peppermint oil aromatherapy in relieving post-operative nausea in the bariatric surgery patient population.


Description:

Healthy weight management and use of essential oils and aromatherapy as natural interventions to manage health-related issues are significantly growing interests. One frequent intervention for healthy weight management is bariatric surgery. In the post-operative period following bariatric surgery, nausea is a common consequence. Peppermint oil aromatherapy is an effective intervention for relieving nausea and other gastrointestinal symptoms in the bariatric and surgical population. This study has multiple aims. One is to determine effectiveness of peppermint oil aromatherapy in relieving post-operative nausea in the bariatric surgery patient population. A second aim is to establish relative cost-effectiveness of peppermint oil aromatherapy versus traditional anti-emetic drug therapies. A third is to determine whether peppermint oil aromatherapy increases patient satisfaction versus anti-emetic drug therapies. This is a randomized study with control and experimental groups. The control group will receive no peppermint oil aromatherapy and only traditional anti-emetics as needed. The experimental group will receive peppermint oil aromatherapy and traditional anti-emetics as needed.


Recruitment information / eligibility

Status Completed
Enrollment 204
Est. completion date December 31, 2019
Est. primary completion date September 10, 2019
Accepts healthy volunteers No
Gender All
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria:

- Bariatric surgery candidate on 7-Lime at Lancaster General Hospital

- Scheduled for laparoscopic sleeve gastrectomy and laparoscopic Roux-En-Y (RNY) procedures

- Between ages of 18 and 70

- Surgical patient of either Dr. James Ku and Dr. Joseph McPhee

Exclusion Criteria:

- History of excessive sensitivity to peppermint oil, allergic response to peppermint oil and who state preference against aromatherapy

- Not alert and oriented or unable to follow directions will be excluded

- Severe reactive airway disease such as asthma or chronic obstructive pulmonary disease (COPD)

- Possible exclusion for severe hypertension or atrial fibrillation

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Peppermint oil aromatherapy
Aroma therapy with peppermint oil administered with presoaked diffuser and bag.

Locations

Country Name City State
United States Lancaster General Hospital Lancaster Pennsylvania

Sponsors (1)

Lead Sponsor Collaborator
Lancaster General Hospital

Country where clinical trial is conducted

United States, 

References & Publications (3)

Anderson LA, Gross JB. Aromatherapy with peppermint, isopropyl alcohol, or placebo is equally effective in relieving postoperative nausea. J Perianesth Nurs. 2004 Feb;19(1):29-35. — View Citation

Lane B, Cannella K, Bowen C, Copelan D, Nteff G, Barnes K, Poudevigne M, Lawson J. Examination of the effectiveness of peppermint aromatherapy on nausea in women post C-section. J Holist Nurs. 2012 Jun;30(2):90-104; quiz 105-6. doi: 10.1177/0898010111423419. Epub 2011 Oct 27. — View Citation

Tate S. Peppermint oil: a treatment for postoperative nausea. J Adv Nurs. 1997 Sep;26(3):543-9. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Nausea Assessment and Treatment Scale Severity of post-operative nausea on a scale of 0-10 4 Hours
Primary Count of Antiemetic Drug Therapies Number of antiemetic drug therapies used in the post-operative period 4 Hours
Primary Perception of Postoperative Nausea Management Survey Patient satisfaction with effectiveness of postoperative nausea management 24 Hours
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