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Study on the effect of inhaled aromatherapy on preoperative anxiety regulation in patients undergoing local anesthesia surgery

Study on the effect of inhaled aromatherapy on preoperative anxiety regulation in patients undergoing local anesthesia surgery

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400091143
Enrollment
Unknown
Registered
2024-10-22
Start date
2024-11-01
Completion date
Unknown
Last updated
2024-10-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

chronic pain

Interventions

Observation group:The patients in the observation group received lavender essential oil inhalation therapy before surgery. One hour before surgery, the observation group dropped 5 drops of 2% lavender
control group:The patients in the control group underwent inhalation of odorless essential oil of the same color before surgery. One hour before surgery, the control group dropped 5 drops of odorless

Sponsors

Fudan University Affiliated Huadong Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 65 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: 1. Age range is 20-65 years old, weighing 45-70kg,with no gender restrictions. 2. Patients undergoing radiofrequency therapy under local anesthesia and ultrasound guidance in the operating room. 3. I have read the instructions for the subjects, agreed to the treatment, and signed a written informed consent form. 4. Willing and able to promptly follow up with patients according to the requirements of the plan.

Exclusion criteria

Exclusion criteria: Exclusion criteria: 1.The anatomical structure of the nasal cavity is abnormal or deformed. 2.In the past two weeks, the patient has a history of upper respiratory tract infection, asthma, mental disorder or epilepsy. 3.Allergic to pollen, plant essence and other substances. 4.Individuals who have recently taken sedatives, undergone emergency surgery, or changed their surgical approach midway should not be included in the study.

Design outcomes

Primary

MeasureTime frame
Anxiety rating;Depression rating;

Secondary

MeasureTime frame
Heart rate variability;Pain rating;Vital sign assessmen;

Countries

China

Contacts

Public ContactDayuan Lu

Fudan University Affiliated Huadong Hospital

664014919@qq.com+86 134 8227 9212

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026