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Effect of Different Heparinization Schemes on Prognosis of Intracranial Aneurysm

Effect of Heparinization on Intracranial Aneurysm

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05749393
Acronym
EODHS-IA
Enrollment
90
Registered
2023-03-01
Start date
2023-04-30
Completion date
2024-04-01
Last updated
2023-12-22

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

Conditions

Intracranial Aneurysm

Keywords

Intracranial Aneurysm

Brief summary

The goal of this clinical trial is to compare intracranial aneurysm patients. The main question it aims to answer are: Which heparinization regimen is most beneficial to patients during surgery for intracranial aneurysms. Participants will be randomized to different intraoperative heparinization regimens: (i) 50 U/kg intravenous (IV) at 1-h intervals reduced by half to a minimum of 1000 u/h; (ii) 70 U/kg IV at 1-h intervals reduced by half to a minimum of 1000 u/h. MRI will be performed within 72 h after surgery, and the DWI sequence of MRI will be analyzed. If there is a comparison group: Researchers will compare different intraoperative heparinization protocol groups to see which dose of intraoperative heparin has the best prognosis for use.

Interventions

Intravenous heparin was administered during intracranial aneurysm embolization with a guide catheter and discontinued at the end of the procedure.

Sponsors

The First Affiliated Hospital with Nanjing Medical University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

1. Greater than 18 years old, less than 75 years old 2. Patients with unruptured intracranial aneurysm were confirmed by DSA. 3. Coagulation function should be normal in the enrolled patients.

Exclusion criteria

1. Dissection aneurysm, blister aneurysm, moyamoya disease or arteriovenous malformation. 2. Previous use of antithrombotic drugs (including anticoagulant or antiplatelet aggregation drugs).

Design outcomes

Primary

MeasureTime frameDescription
Size of the ischemic focusThis will be evaluated within 24 hours after the procedure.Cranial MRI will be performed on postoperative patients within 24 hours. The presence of high signal on diffusion weighted imaging sequences indicated the occurrence of cerebral infarction.

Countries

China

Contacts

Primary ContactHua Lu, Doctor
luhua@njmu.edu.cn18761671021

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026