Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
ID07281885

A Randomized Control Trial on the Efficacy of Aromatherapy in Reducing Postoperative Nausea and Vomiting in Total Joint Replacement Patients

Led by Hong Kong Buddhist Hospital · Updated on 2026-01-07

159

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

Sponsors

H

Hong Kong Buddhist Hospital

Lead Sponsor

Q

Queen Elizabeth Hospital, Hong Kong

Collaborating Sponsor

AI-Summary

What this Trial Is About

Researchers are evaluating the effectiveness of aromatherapy in reducing postoperative nausea and vomiting (PONV) among patients undergoing total joint replacement surgery. This randomized controlled trial involves 159 participants divided into three groups to assess if aromatherapy can improve postoperative care and patient satisfaction as a complementary treatment to standard antiemetic therapies. Participants will be assigned to one of three groups: one receiving aromatherapy patches (lavender-sandalwood or orange-ginger) along with standard care, one receiving placebo patches plus standard care, and a control group receiving only standard prescribed antiemetic treatment. Aromatherapy or placebo patches are applied to the inner side of the patient's top, covered by gauze and micro-pore tape. The intervention and follow-up occur over approximately 24 hours post-surgery. During the study, patients' nausea and vomiting will be measured using the Rhodes Index of Nausea, Vomiting, and Retching (RINVR) at baseline, 30 minutes after patch application, and at 12 and 24 hours after surgery. Patient satisfaction will also be assessed with a 5-point Likert scale. Data will be analyzed statistically to understand the effects of aromatherapy on PONV and satisfaction, with careful monitoring throughout the study period.

CONDITIONS

Brief Title

Aromatherapy in Reducing PONV for Total Joint Replacement Patients

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults aged 18 or above
  • Patients scheduled for total joint replacement surgery at the HKBH
Not Eligible

You will not qualify if you...

  • Cognitive impairments
  • Allergy to lavender, orange, ginger, or sandalwood
  • Allergy to micro-pore tape
  • Allergy to opioid medication
  • Undergoing other therapeutic treatment for PONV control, except prescribed medications

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

1
2
3
+1

Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

Duration - Approximately 24 hours following surgery

Participants receive standard care for total joint replacement surgery and are randomly assigned to receive either aromatherapy patches, placebo patches, or prescribed antiemetic treatment to reduce postoperative nausea and vomiting.

4 assessments during the first 24 hours post-surgery at specified timepoints: baseline (PACU), 30 minutes after intervention, 12 hours post-intervention, and 24 hours post-intervention

Trial Site Locations

Total: 1 location

1

Hong Kong Buddhist Hospital

Wong Tai Sin, Hong Kong, Hong Kong

Actively Recruiting

Loading map...

Research Team

C

Choi Wan CHAN, APN (NURSING)

V

Victor CHEUNG, EOII(MDSSC)

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

3

Similar Trials

A Comparison Between Palonosetron Versus Granisetron As Post...

Postoperative Nausea and Vomiting

Actively Recruiting

2 locations

Association Between Preoperative Metformin Exposure and Post...

Postoperative Nausea and Vomiting

Actively Recruiting

1 location

Intravenous Dexamethasone Palmitate for Prophylaxis of Posto...

Postoperative Nausea and Vomiting

Actively Recruiting

1 location

Frequently Asked Questions

Have more questions? Get in touch with our team for quick support

Not the Right Trial for You?

Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.

Already have an account? Log in here

Published Research Related To This Trial

The efficacy of ginger for the prevention of postoperative nausea and vomiting: a meta-analysis.

Nathorn Chaiyakunapruk, Nantawarn Kitikannakorn, Surakit Nathisuwan...

https://pubmed.ncbi.nlm.nih.gov/16389016

Assessing the psychometric and language equivalency of the Chinese versions of the Index of Nausea, Vomiting and Retching, and the Prenatal Self-Evaluation Questionnaire.

Fan-Hao Chou, Kay C Avant, Shih-Hsien Kuo...

https://pubmed.ncbi.nlm.nih.gov/16089309

Effect of Lavender (Lavandula angustifolia) Essential Oil on Acute Inflammatory Response.

Gabriel Fernando Esteves Cardia, Saulo Euclides Silva-Filho, Expedito Leite Silva...

https://pubmed.ncbi.nlm.nih.gov/29743918

Prevention and Treatment of Postoperative Nausea and Vomiting (PONV): A Review of Current Recommendations and Emerging Therapies.

Zhaosheng Jin, Tong J Gan, Sergio D Bergese

https://pubmed.ncbi.nlm.nih.gov/33408475