Neuroprotectant for Hypertensive Intracerebral Hemorrhage
Fjalë kyçe
Abstrakt
Përshkrim
Hypertensive intracerebral hemorrhage (HICH) is a type of stroke that is caused by hypertension-induced intracranial arterial, venous, and capillary ruptures. In recent years, the incidence of HICH has become higher, which has exposed society greatly to heavy social and economic burdens. Therefore it is necessary to find therapeutic strategies. ICH causes primary white matter injury by direct mechanical compression and hematoma expansion, and then it induces secondary injury through toxic product from the blood out of the vessel. The inflammatory response that follows ICH also contributes to the white matter injury. Additionally, post-ICH complications that include cortical thinning, cerebral edema, and hydrocephalus further aggravate the subcortical white matter damage.
The complex injury mechanisms that follow ICH implies that a multi-target neuroprotective agent might be able to achieve better neuroprotective effects than current single-agent neuroprotective therapies.
Cattle encephalon glycoside and ignotin Cattle encephalon glycoside and ignotin (CEGI) injection (drug approval H22025046; Jilin Sihuan Pharmaceutical Co. LTD., Jilin, People's Republic of China) is a multi-target neuroprotective agent that includes polypeptides, various gangliosides, free amino acids and nucleic acids, which were extracted from muscle tissue of healthy rabbits and cattle brain gangliosides, and was approved by the Chinese Food and Drug Administration in 2011, commonly used as neuroprotectant in the treatment of central and peripheral nerve injuries in China.
It has been proven by basic research that CEGI treatment significantly alleviated the neurobehavioral dysfunction, promoted hematoma absorption, effectively up-regulated MBP/MAP-2 expression, and ameliorated white matter fiber damage [1]. CEGI was frequently used in the treatment of intracerebral hemorrhage, yet there is still a lack of high quality study to demonstrate its clinical efficacy. To achieve more clinical evidence of CEGI in treatment of Hypertensive intracerebral hemorrhage, we designed this study to further evaluate the efficacy and safety of CEGI in the treatment of Hypertensive intracerebral hemorrhage.
Datat
| Verifikuar së fundmi: | 05/31/2018 |
| Paraqitur së pari: | 05/15/2018 |
| Regjistrimi i vlerësuar u dorëzua: | 06/02/2018 |
| Postuar së pari: | 06/05/2018 |
| Përditësimi i fundit i paraqitur: | 06/02/2018 |
| Përditësimi i fundit i postuar: | 06/05/2018 |
| Data e fillimit të studimit aktual: | 06/14/2018 |
| Data e vlerësuar e përfundimit primar: | 07/30/2020 |
| Data e vlerësimit të përfundimit të studimit: | 12/30/2020 |
Gjendja ose sëmundja
Ndërhyrja / trajtimi
Drug: Control
Drug: CEGI treatment
Faza
Grupet e krahëve
| Krah | Ndërhyrja / trajtimi |
|---|---|
| Placebo Comparator: Control The patients with hypertensive intracerebral hemorrhage will be randomized into giving placebo group, the other treatments in this group follow the guidelines on the treatment of hypertensive intracerebral hemorrhage. | Drug: Control The patients with hypertensive intracerebral hemorrhage will be randomized into giving placebos, the other treatments in this group follow the guidelines on the treatment of hypertensive intracerebral hemorrhage. |
| Experimental: CEGI treatment The patients with hypertensive intracerebral hemorrhage will be randomized into giving drug CEGI, the other treatments in this group follow the guidelines on the treatment of hypertensive intracerebral hemorrhage. | Drug: CEGI treatment The patients with hypertensive intracerebral hemorrhage will be randomized into giving CEGI, the other treatments in this group follow the guidelines on the treatment of hypertensive intracerebral hemorrhage. |
Kriteret e pranimit
| Moshat e pranueshme për studim | 18 Years Për të 18 Years |
| Gjinitë e pranueshme për studim | All |
| Pranon Vullnetarë të Shëndetshëm | po |
| Kriteret | Inclusion Criteria: 1. Individuals aged 18-75 years; 2. Newly diagnosed hypertensive intracerebral hemorrhage, bleeding position localizes in Basal ganglia and bleeding volume is within 25-50ml evaluated by head CT, and the hemorrhage does not break into lateral ventricle; 3. Obvious neurological dysfunction after onset, Glasco Comma Scale evaluation between 5-14, or NIHSS above 6, but without signs of cerebral hernia. 4. Enrolled within 72 hours after onset, and CT examination shows no hematomas expansion within 6 hours or above after diagnostic CT (hematoma expansion ≤ 5ml); 5. Written informed consent can be obtained. Exclusion Criteria: 1. Diagnosed with intracerebral hemorrhage caused by aneurysm, brain tumor, trauma, cerebral parasitic disease, cerebrovascular malformation, moyamoya disease, cerebral arteritis, hematological diseases, or metabolic disorders; 2. Patients whose hematoma is unstable or progress leading to increased intracranial pressure; 3. Ever diagnosed with subarachnoid hemorrhage and ischemic stroke; 4. Ever received anticoagulants or antiplatelet drug treatment within one month prior to onset; 5. Abnormal coagulation function (platelet count <100×109/L, INR>1.4); 6. Patients who need operation treatment (including external ventricular drainage); 7. Patients who may suffer from mental or physical diseases that disturb outcome evaluation; 8. blood homocysteine higher than 15μmol/L when admission; 9. Patients who have serious diseases in heart, lung, liver, kidney, endocrine or hemopoietic system; 10. Allergic to protein or peptide; 11. Drug or alcohol addiction; 12. Pregnant women (positive in pregnancy test or lactating women) 13. Participated in other clinical trials within 3 months; 14. Patients considered as not suitable for clinical trials by researchers. |
Rezultati
Masat Kryesore të Rezultateve
1. GOSE at 90 days [90 days after onset]
Masat dytësore të rezultateve
1. GOSE at 30 days [30 days after onset]
2. Score of mRS at 14days, 30 days and 90 days [14 days, 30 days and 90 days after onset]
3. Score of NIHSS at 14days, 30 days and 90 days [14 days, 30 days and 90 days after onset]
4. Score of Barthel Index at 14days, 30 days and 90 days [14 days, 30 days and 90 days after onset]
5. Complications [within 90 days after onset]
