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

Phase 3

Recruiting

• Conditions: Preoperative Period; Postoperative Period; Pain, Postoperative; Preoperative Care; Postoperative Care; F41.1

• Registration Number: RBR-1085kmg5
• Lead Sponsor: Hospital Universitário Onofre Lopes da Universidade Federal do Rio Grande do Norte

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2024-08-07
• Last Update Posted: 19 August 2024
• Study Completion: 2025-03-31

Recruitment & Eligibility

• Status: Recruiting
• Sex: Not specified
• Target Recruitment: Not specified

Inclusion Criteria

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

Exclusion Criteria

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

Study & Design

• Study Type: Intervention
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Preoperative anxiety reduction measured through the VAS (Visual Analog Scale).<br>

Secondary Outcome Measures

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