Effect of Lavander on preoperative Anxiety and postoperative Pain: randomized clinical trial

Effect of Lavandula Angustifolia on preoperative Anxiety and postoperative Pain: randomized clinical trial

Status

Recruiting

Phases

Phase 3

Study type

Interventional

Source

REBEC

Registry ID

RBR-1085kmg5

Enrollment

Unknown

Registered

2024-08-07

Start date

2024-05-06

Completion date

Unknown

Last updated

2025-10-27

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

Conditions

Preoperative Period

Interventions

This is a double-blind randomized clinical trial. A total of 140 participants will be included in the study, with 70 in the intervention group who will receive lavender (Lavandula angustifolia) and 70

B01.875.800.575.912.250.583.520.428

Eligibility

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: Individuals of both genders; aged 18 and over; who will undergo elective surgical procedures in the field of otolaryngology

Exclusion criteria

Exclusion criteria: Presence of reported or confirmed dementia; patients on mechanical ventilation; tracheostomized patients; and previous skull base surgery

Design outcomes

Primary

Measure	Time frame
Preoperative anxiety reduction measured through the VAS (Visual Analog Scale).	—

Secondary

Measure	Time frame
Analgesic use and postoperative pain reduction measured via VAS (Visual Analog Scale).;Change in the the portuguese validated questionnaire for preoperative anxiety (APAIS).	—

Countries

Brazil

Contacts

Public ContactLidiane Maria Ferreira

Hospital Universitário Onofre Lopes da Universidade Federal do Rio Grande do Norte

proflidianeotorrino@gmail.com+55(84)33425041

Outcome results

None listed

Source: REBEC (via WHO ICTRP)