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Study identifier: NCT07732036 Synced from ClinicalTrials.gov · August 08, 2026
● Study status: Recruiting

Inhalation Aromatherapy for Patients Undergoing Conservative Sharp Wound Debridement:

Condition: Aromatherapy  ·  Sponsor: Singapore General Hospital

PhaseNA
Planned participants40
Who can joinAll sexes, 21 Years to 21 Years
Healthy volunteersNoCheck eligibility criteria ↓
Where2 locations

Interested? Contact the study team ↓

Sponsor, CRO or site team? See where this study is running → — listed sites, countries and recruiting context. Everything below is written for patients and caregivers.

About this study

The goal of this pilot clinical trial is to learn if inhalation aromatherapy works to reduce anxiety and pain in patients with venous leg ulcers undergoing conservative sharp wound debridement (CSWD). It will also learn about the feasibility of implementing this intervention in clinical practice. The main questions it aims to answer are: Does inhalation aromatherapy reduce anxiety levels during CSWD procedures, as measured by STAI-S scores? Does inhalation aromatherapy reduce pain intensity during CSWD procedures? Is inhalation aromatherapy feasible and acceptable to implement in a clinical setting? What are the protocol adherence rates and potential areas of missing data? Researchers will compare inhalation aromatherapy using Asian essential oil extracts to standard care to see if aromatherapy works to reduce anxiety and pain during wound debridement. Participants will: Receive either inhalation aromatherapy or standard care during their CSWD procedure Complete State-Trait Anxiety Inventory (STAI-S) questionnaires before and after the procedure Rate their pain intensity using visual analog scales during the debridement Provide feedback on treatment satisfaction and acceptability Attend clinic visits for wound debridement as part of their standard care This pilot study hypothesizes that inhalation aromatherapy is feasible and acceptable to implement in a clinical setting and may be associated with differences in anxiety and pain intensity during CSWD, compared to standar…

This description comes directly from the study's public registry record.

Talk to the study team

Nanthakumahrie Gunasegaran  ·  97250435  ·  nanthakumahrie.gunasegaran@sgh.com.sg

There is no obligation to join — the study team can answer your questions about taking part.

Always discuss trial participation with your own doctor first.

Full eligibility criteria (exactly as the study team wrote them)

Inclusion Criteria: -≥21 years old -Venous leg ulcers requiring conservative sharp wound debridement Exclusion Criteria: * Known sensitivity or hypersensitivity to essential oils or any components in the Aromatherapy scent formulation * Allergic rhinitis, asthma, chronic lung disease or any disease that impairs the sense of smell * Airway hypersensitivity to fragrances, paint/gasoline fumes or turpentine * Using aromatherapy of any kind * Taking any anti-psychotic drugs * Incapable of providing verbal/written consent * On anti-anxiety medications

Reproduced word-for-word from the public registry record — the study team can answer questions about it.

Locations (2)

Singapore General HospitalSingapore, SingaporeRecruiting
Singapore General HospitalSingapore, SingaporeRecruiting

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This study lists sites in the areas below. Each link shows other recruiting studies near that city, from the public registry record.

Singapore

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