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Clinical Trials/IRCT20240511061733N1
IRCT20240511061733N1
Recruiting
未知

The effect of massage aromatherapy with lavender oil on physiological indicators and pain intensity caused by the change position of patient with cerebrovascular accident admitted to the intensive care unit

Artesh University of Medical Sciences0 sites81 target enrollmentTBD

Overview

Phase
未知
Intervention
Not specified
Conditions
Physiological indicators and pain caused by changes in the condition of patients with cerebrovascular accidents.
Sponsor
Artesh University of Medical Sciences
Enrollment
81
Status
Recruiting
Last Updated
last year

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
last year
Study Type
Interventional
Sex
All

Investigators

Sponsor
Artesh University of Medical Sciences

Eligibility Criteria

Inclusion Criteria

  • 1\_ Patients with a cerebrovascular accident confirmed by a physician 2\_ Age over 65 years 3\_ Patients without a history of asthma and chronic respiratory disease 4\_ Patients without a history of allergy to lavender based on the statement of the patient or the patient's companion 5\_ Patients without a history of olfactory disorders 6\_ Patients without a history of psoriasis 7\_ Absence of drug addiction 8\_ Patients without intubation in the trachea 9\_ Healthy skin of the hands 10\_ Being hospitalized in the intensive care unit for at least 24 hours 11\_ Patient not using painkillers, narcotics and sedatives 6\-8 hours before, while and after the intervention 12\- Not having an angioket at the massage site 13\- Patients without receiving drugs that increase or decrease blood pressure such as: epinephrine, dopamine, dobutamine, TNG, etc. 14\- Patients without receiving anticonvulsant drugs such as: Gabapentin

Exclusion Criteria

  • 2\_The patient's sensitivity to lavender during the intervention 3\_Irritation and skin damage in the hands area during the study 4\_Instability and sudden changes in the patient's condition 5\_The need to intubate the patient during the study

Outcomes

Primary Outcomes

Not specified

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