About this trial
The purpose of this study is to dynamically observe the dynamic changes of serum IGF-1 after intracerebral hemorrhage, explore the impact and correlation of serum IGF-1 with the severity of the patient's condition and prognosis, and provide a reference for clinical treatment timing.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Aged 18 to 75 years old;
Patients with intracerebral hemorrhage (NIHSS ≥5 points);
No history of cerebrovascular diseases with residual functional impairment before brain injury;
Hospitalized within 72 hours after injury;
Disqualifiers
Patients with severe cardiac, hepatic, renal, or pulmonary dysfunction;
Glycated hemoglobin >9.0% at screening;
History of hypothalamic-pituitary related diseases or severe endocrine diseases;
Use of drugs affecting endocrine function (such as glucocorticoids, growth hormones) within the past six months;
Trial population
Patients with intracerebral hemorrhage from Shengjing Hospital Affiliated to China Medical University and those from Northern Theater General Hospital
Trial design
Other
Prospective
Treatments tested in this trial
Not listed
Trial groups
Trial outcomes
Primary outcomes
The relationship between serum IGF-1 levels within 3 days after intracerebral hemorrhage and the severity of the condition (referring to NIHSS score)
Serum IGF-1 levels decrease in the acute phase after intracerebral hemorrhage, and the decrease is correlated with the severity of the condition. (The more severe the condition, the larger the number of patients with reduced IGF-1 levels, and the more significant the decrease in IGF-1 values.),The higher the IGF-1 level, the lower the NIHSS score.
Secondary outcomes
The correlation between the dynamic change trend of IGF-1 after intracerebral hemorrhage and the prognosis of patients
Patients with persistently decreasing IGF-1 levels have worse functional prognosis than those with persistently normal IGF-1 levels.
Locations
Sponsors and contacts
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