Actively Recruiting
Aromatherapy in Reducing PONV for Total Joint Replacement Patients
Led by Hong Kong Buddhist Hospital · Updated on 2026-01-07
159
Participants Needed
1
Research Sites
65 weeks
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
This study investigates the effectiveness of aromatherapy in reducing postoperative nausea and vomiting (PONV) among patients undergoing total joint replacement surgery, as these complications can lead to patient discomfort and prolonged recovery. It is designed as a randomized controlled trial involving 159 participants, who will be divided into three groups: an intervention group receiving aromatherapy patches (lavender-sandalwood or orange-ginger) plus standard care, a placebo group with a placebo patch plus standard care, and a control group receiving standard care alone. PONV will be measured using the Rhodes Index of Nausea, Vomiting, and Retching (RINVR) at baseline, 30 minutes after the intervention, and every 12 hours post-surgery. Additionally, patient satisfaction will be assessed through a 5-point Likert scale survey. The primary outcome of the study is the evaluation of RINVR scores, while the secondary outcome focuses on patient satisfaction levels. Data will be statistically analyzed using two-way ANOVA for repeated measures, with a significance level defined as p \< 0.05. The study aims to determine the viability of aromatherapy as a complementary treatment for PONV, potentially improving postoperative care, enhancing patient satisfaction, and offering a cost-effective alternative to conventional anti emetic treatments if proven effective.
CONDITIONS
Official Title
Aromatherapy in Reducing PONV for Total Joint Replacement Patients
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adults aged 18 or above
- Patients scheduled for total joint replacement surgery at the HKBH
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
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Trial Site Locations
Total: 1 location
1
Hong Kong Buddhist Hospital
Wong Tai Sin, Hong Kong, Hong Kong
Actively Recruiting
Research Team
C
Choi Wan CHAN, APN (NURSING)
CONTACT
V
Victor CHEUNG, EOII(MDSSC)
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
3
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