level of consciousness. Other coma, without documented Glasgow coma scale score, or with partial score reported
Conditions
Interventions
Intervention 1: Intervention group: Twenty-one patients with a diagnosis of spontaneous bleeding after random allocation will be included in this study. After being admitted to the relevant ward, defe
Sponsors
Tabriz University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to 75 Years
Inclusion criteria
Inclusion criteria: Brain stroke Spontaneous cerebral hemorrhage Satisfaction to participate in the study
Exclusion criteria
Exclusion criteria: Requires brain surgery Stroke over the last six months Hypersensitivity to deferoxamine
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Level of consciousness. Timepoint: Before the intervention, one week and one month after the end of the intervention. Method of measurement: With the help of GCS criteria. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactMohammad Shimia
Tabriz University of Medical Sciences
Outcome results
None listed