Effect of Inhalation of Mint Oil on Vital Signs and O2 Saturatio

Phase 2

Recruiting

Conditions: Condition 1: neurosurgery Patient Hospitalized in Intensive Care Unit. Condition 2: neurosurgery Patient Hospitalized in Intensive Care Unit. Condition 3: neurosurgery Patient Hospitalized in Intensive Care Unit.
Epidural hemorrhage
Traumatic subdural hemorrhage
Diffuse traumatic brain injury
S06.4X
S06.5X
S06.2

Registration Number: IRCT20210131050189N1

Lead Sponsor: Shahid Beheshti University of Medical Sciences

Brief Summary: Not available

Detailed Description: Not available

Recruitment & Eligibility

Status: Recruiting

Sex: All

Target Recruitment: 80

Inclusion Criteria

Age over 18 years and under 50 years
No history of allergy to a particular substance-
Awareness level above 13 according to Glasgow criteria
No history of addiction
No underlying disease (diabetes, high blood pressure, chronic heart failure, respiratory failure and kidney failure)-
No endotracheal tube or 24 hours after extubation
Stability of vital signs at least 12 hours before the extubation

Exclusion Criteria

Any sudden change in vital signs and general condition during the intervention that is a sign of intolerance to aromatherapy.
Any change in the patient's breathing pattern during the intervention
Change in the patient's medication during the intervention up to 6 hours after the intervention
Complications after surgery such as severe pain, active bleeding, or infection

Study & Design

Study Type: interventional

Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Blood pressure. Timepoint: 6 hours after intervention. Method of measurement: blood pressure monitoring.;O2 Saturation. Timepoint: 6 hours after intervention. Method of measurement: pulse oximetry.;Pulse rate. Timepoint: 6 hours after intervention. Method of measurement: heart rate monitoring.;Respiratory rate. Timepoint: 6 hours after intervention. Method of measurement: respiratory rate monitoring.

Secondary Outcome Measures