delirium. Other delirium ( Postoperative delirium)
Conditions
Interventions
Intervention 1: Intervention group:In the intervention group, patients receive an oral supplement dose of Yarrow capsule of 500 mg (the product includes the composition of Yarrow extract, microcrystal
Sponsors
Rafsanjan University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to 70 Years
Inclusion criteria
Inclusion criteria: Consent of the patient or consent of the first degree of the patient to participate in the study Age 18-70 years of both sexes Family availability Not having a history of blindness and deafness Score 10-18 in SOFA criteria Insensitivity to herbal medicines Obtaining a score higher than 12 in the GCS criterion Absence of pregnancy No use of chemical drugs to treat delirium Absence of predetermined cognitive diseases such as: delirium, dementia, Alzheimer's, schizophrenia, loss of memory and attention. No alcohol consumption
Exclusion criteria
Exclusion criteria: Lack of consent to continue participating in the study Death or discharge of the patient before completion of the study Decreased level of consciousness and need for mechanical ventilation Not taking yarrow oral supplement or placebo for three consecutive days Allergy to herbal medicines (dermatitis)
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The score of the CAM ICU questionnaire. Timepoint: Once every 24 hours. Method of measurement: CAM ICU questionnaire. | — |
Secondary
| Measure | Time frame |
|---|---|
| The amount of score received from the CAM ICU questionnaire. Timepoint: Once every 24 hours. Method of measurement: CAM ICU questionnaire. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactMajid Kazemi
Rafsanjan University of Medical Sciences
Outcome results
None listed