Study on Dynamic Changes of Serum IGF-1 Post-Cerebral Hemorrhage and Its Prognostic Correlation

Not yet recruiting

• Conditions: Insulin-Like Growth Factor I

• Registration Number: NCT07043504
• Lead Sponsor: Shengjing Hospital

Brief Summary

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.

Detailed Description

Research Objectives

1. Monitor the dynamic changes in serum IGF-1 concentration in patients with intracerebral hemorrhage at different time points (within 3 days, 14 days, 1 month, 2 months, and 4 months after onset).

2. Analyze the correlation between serum IGF-1 levels and the severity of intracerebral hemorrhage, imaging findings, and prognosis.

3. Explore the clinical value of serum IGF-1 as a biomarker for intracerebral hemorrhage repair.

4. Provide a reference for the clinical treatment timing of IGF-1-related drugs and therapies (such as rh growth hormone, rhIGF-1, etc.).

Experimental Methods

Screening Period:

Within 3 days after onset, record the demographic data, etiology, medical history, complications, disease course, and main clinical manifestations of the subjects during the screening period. Blood sampling for laboratory tests (between 06:00-08:00 in the morning within 3 days after onset) includes: complete blood count, IGF-1, GH, IGFBP-3, LDL-C, thyroid function T4, serum cortisol, ACTH, testosterone or progesterone, serum CRP, fasting blood glucose, glycated hemoglobin. Perform head CT and NIHSS scoring.

Follow-up Period:

At the 15th day, 1st month, and 2nd month of the subject's disease course:

Conduct laboratory tests for IGF-1, GH, and IGFBP-3. Evaluate using the Modified Barthel Index (MBI), Modified Rankin Scale (MRS), Glasgow Coma Scale (GCS), Mini-Mental State Examination (MMSE), PHQ-9 Depression Screening Scale (PHQ-9), and World Health Organization Quality of Life-BREF (WHOQOL-BREF).

At the 4th month of the subject's disease course:

Perform laboratory tests for complete blood count, IGF-1, GH, IGFBP-3, LDL-C, thyroid function T4, serum cortisol, ACTH, testosterone or progesterone, CRP, fasting blood glucose, and glycated hemoglobin.

Evaluate using the same scales as above (MBI, MRS, GCS, MMSE, PHQ-9, WHOQOL-BREF).

Grouping Based on Dynamic Changes in Serum IGF-1:

Convert IGF-1 values to IGF-1 SD (standard deviation) by referencing the age-specific reference values for IGF-1 in healthy Chinese populations (Peking Union Medical College).

IGF-1 Decreased Group: IGF-1 \< 0SD IGF-1 Normal Group: 0SD ≤ IGF-1 ≤ 2SD

Dynamic change-based grouping:

① Persistent IGF-1 Decrease Group: IGF-1 remains \< 0SD throughout dynamic observation.

② IGF-1 Decrease to Normal Group: IGF-1 first \< 0SD, then recovers to \> 0SD.

③ Persistent IGF-1 Normal Group: IGF-1 remains \> 0SD throughout dynamic observation.

Statistical Analysis Based on Experimental Data

Study Timeline

• Status Verified: 2025-06
• Study First Submitted: 2025-06-21
• Study First Submitted QC: 2025-06-21
• Last Update Submitted: 2025-06-21
• Study First Posted: 2025-06-29
• Last Update Posted: 2025-06-29
• Study Start: 2025-07-01
• Primary Completion: 2026-12-31
• Study Completion: 2026-12-31

Recruitment & Eligibility

• Status: NOT_YET_RECRUITING
• Sex: All
• Target Recruitment: 100

Inclusion Criteria

1. Aged 18 to 75 years old;
2. Patients with intracerebral hemorrhage (NIHSS ≥5 points);
3. No history of cerebrovascular diseases with residual functional impairment before brain injury;
4. Hospitalized within 72 hours after injury;
5. BMI ≤28.

Exclusion Criteria

1. Patients with severe cardiac, hepatic, renal, or pulmonary dysfunction;
2. Glycated hemoglobin >9.0% at screening;
3. History of hypothalamic-pituitary related diseases or severe endocrine diseases;
4. Use of drugs affecting endocrine function (such as glucocorticoids, growth hormones) within the past six months;
5. Pregnant patients. -

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
The relationship between serum IGF-1 levels within 3 days after intracerebral hemorrhage and the severity of the condition (referring to NIHSS score)	3 days after intracerebral	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 Outcome Measures

Name	Time	Method
The correlation between the dynamic change trend of IGF-1 after intracerebral hemorrhage and the prognosis of patients	The 5th month	Patients with persistently decreasing IGF-1 levels have worse functional prognosis than those with persistently normal IGF-1 levels.