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Effect of Albumin in Stroke

Assessment the effect of ALBUMIN compared with PLACEBO on functional outcome after Ischemic Stroke in18-83 year old patients with Ischemic Stroke inMCA territory referred to Golestan hospital of Ahvaz

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201008214606N1
Enrollment
140
Registered
2012-05-13
Start date
2010-01-21
Completion date
Unknown
Last updated
2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Ischemic Stroke. Cerebral infarction due to thrombosis of cerebral arteries

Interventions

Intervention 1: 20% Vial Albumin 1 geram per kiloogram Body Weight infusion during 2 hours Single Dose. Intervention 2: Plasebo Vial as a Same Dose of Albumin.
Treatment - Drugs
Placebo
20% Vial Albumin 1 geram per kiloogram Body Weight infusion during 2 hours Single Dose
Plasebo Vial as a Same Dose of Albumin

Sponsors

JondiShapur Ahvaz university of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 83 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: patients with acute ischemic stroke; age between 18 to 83 years old; NIH stroke scale more than 5; transfusion of albumin with in 5 hour and infarction in MCA area. Exclusion criteria: heart failure(CHF) in 6 last months; concurrent valvular heart disease with CHF; stenosis of aorta or aortic valve; open heart surgery; acute MI in last 6 month; MI symptoms; Troponin increase in hospitalization (>0.1mcg/l); doubt of aorta dakshin in hospitalization; acute heart arythmia cause of hemodynamic transience; physical examination results include: JVP>4cm on top of sternal angle S3, Tachycardia in relaxation cause Congestive Heart failure (HR>100/min), hepatojugular abnormal reflex specific C-xray of Pulmonary edema Pitting edema of the lower extremities that can cause congestive heart failure; acute or chronic lung disease requiring supplemental oxygen therapy is intermittent or permanent; fever T>37.5; serum creatinine > 2 mg / dl.; excessive dehydration; evidence of cerebral hemorrhage on CT or MRI (Intracranial hematoma / SAH / epidural hemorrhage / acute or chronic subdural hematoma); allergy to albumin 17.Allery to latex; Hgb < 7.5 g / dl; pregnancy / lactation / positive pregnancy test (women of childbearing age have a negative test for pregnancy before albumin administration ); medical evidence of any serious or life-threatening condition that interfere with 3-month follow-up trial or assessing patients'outcome or Treatment with the contraindica albumin is harmful; participation in another clinical trial data yet; occurrence of stroke due to complications of hospitalization for other conditions or complications due to a procedure; not afford to buy albumin and lacunar Infarction.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Patient Functional Outcome. Timepoint: At admission time,after one week and after 3 month. Method of measurement: Barthel Scale, Modified Rankin Scale.

Secondary

MeasureTime frame
Morbidity and Mortality. Timepoint: At the admision, after one week and 3 month. Method of measurement: Registration of mortality.;Drug side effects. Timepoint: At the admision,after one week and 3 month. Method of measurement: Drug side effects chart.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAhmad Hemmati, MD

JondiShapurAhvaz University of Medical Sciences

hemmati.ahmad@yahoo.com+98 61 1374 3012

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026