Prospective, Multicenter Cohort Study on the Safety and Efficacy of Treatment for Middle Cerebral Artery Aneurysms

1. Data collection and management A unified and open public health platform will be established, and data will be centrally recorded in each central unit for verification by inspectors. An open network data platform for intracranial aneurysm research was established by the management personnel of different qualification levels. In order to ensure the advancement and sustainable development of the data platform construction, a public research platform for intracranial aneurysms shared in the province was built by using the keywords and retrieval items commonly used in China. After researcher training and standardized study of the scheme, the formal trial was started. A team of experts will be selected to form an inspection team, which will initiate visits to each organization and conduct the first inspection visit as soon as possible after screening the first subject. Regular monitoring visits are required until the end of the experiment. All the data were collected according to the electronic medical record (CRF) form, and then the aneurysm data (EDC) was managed according to the CRF form, and the accuracy and rigor of the data were checked in time. This study establishes a management committee, including clinical experts, evidence-based medicine experts, and CRO clinical study supervisors, who are responsible for project design, task formulation, supervision of project implementation, data analysis and formulation of standards and guidelines. The central laboratory and imaging interpretation center were established to carry out unified standard central storage for clinical specimens. The unified image and laboratory technology platform can be used for the image examination and post-processing technology in the project. Uniform standard interpretation of imaging data was carried out. A unified, standardized and efficient transmission mechanism for clinical specimens, data and data in each center was established. Establish a data management committee, set up a network data platform and be responsible for the construction and maintenance of the database, conduct real-time supervision on the quality of the input data, ensure the safety, integrity and accuracy of the data, establish and organize the implementation of the platform or offline dual-channel error correction and reminder mechanism. Set and manage the rights of all project participants on the data platform, monitor and record the data entry, modification and retrieval, set and manage the data publication of the open platform. Contact and consult statistical experts to conduct periodic analysis of data results and generate research reports. Relying on professional CRO company, in the implementation process for the implementation of the progress and quality of the implementation of random inspection supervision. At the same time, set up a data regular self-check mechanism. Establish a mechanism for regular training and evaluation of research participants. During the research progress, regular project coordination meetings were held to timely coordinate and solve problems in the process of the project. 2. Sample size Sample size was calculated according to a calculation formula (α=0.05, bilateral test, 80% assurance). According to the literature and the data of the center, the rate of MRS\<2 at 3 months was 95% for patients with endovascular interventional, and was 85% for those with craniotomy and clipping. The number of samples needed for each group was calculated by the software PASS15 to be at least 141. Considering that the maximum shedding rate of 20% might occur during the clinical follow-up, 180 cases were needed for each group, and 360 subjects were finally decided to be included in the study. 3. Statistical Methods Statistical analysis of planned primary and secondary study endpoints will be conducted in accordance with the intentionality treatment principle. Subgroup analysis According to the needs of the experiment, the subjects can be divided into different centers, male and female, and different age groups for corresponding subgroup analysis. Methods for processing lost data Statistical analysis did not follow the study protocol population definition and other statistical methods were used to deal with lost data (e.g. multiple interpolation). 4. Ethical approval of clinical research projects The study plan was reviewed and approved by the Ethics Committee of the Second Affiliated Hospital of Zhejiang University School of Medicine. The study protocol was designed and implemented in accordance with the International Conference on Harmonization for Good Clinical Practice (ICH-GCP) guidelines. In line with the national ethical behavior requirements, applicable to local laws and regulations, in strict compliance with the World Medical Association (WMA) Declaration of Helsinki ethical provisions. 5. Informed Consent Process Improve the relevant examinations, check the inclusion and exclusion criteria of patients, and send the detailed information of the study to patients or their legal clients. If the patients or legal clients agree to participate in the study, they need to sign two copies of informed consent. The original consent form should be kept in the patient's study folder and another copy given to the patient. Patients or legal clients have the right to terminate their participation in the study at any time, and their decision will be recorded in the patient's study record. 6. confidentiality The investigators will take every step to respect the privacy of the participants in the study. Only data that does not contain identifying information will be entered into the central research database to ensure the privacy of participants. In the process of monitoring data quality and study protocol compliance, the data monitor will refer to the medical records of the subject's clinical center and record them on the patient information sheet. In the reporting data and results, all personal information and research center information will be hidden to protect the privacy of participants. 7. Adverse events management Adverse events occurred in the process of adverse events refers to the study of the subjects has a harmful effect on the health of all events. Serious Adverse Event Category: Serious Adverse Event refers to any event that occurred during the course of the study that had a serious adverse effect on the health of the subjects. Include: cause the subject to be hospitalized, prolong the length of the subject's hospital stay, cause the subject to be disabled, cause the subject's neurological or physical dysfunction, cause the subject's offspring to be born with a deformity, endanger the subject's life, the subject's death or other events that have a serious adverse effect on the subject's health. Adverse events reported to process all kinds of adverse events: take timely measures to deal with, and recorded in a report on the case. Serious adverse event (SAE) : take timely measures to deal with, and recorded in a report on the case, the researchers decided to withdrawal or by drugs, immediately report ethics committee, the drug clinical trial institution and the sponsor, 24 hours, report to the national and provincial food and drug administration. SAE is required to report adverse events and proximate errors via the Intra-hospital Network Notification System.