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Clinical Trials in China / NCT06459427
Recruiting Not applicable

A Multicenter, RAndomIzed, coNtrolled, umBrella Trial fOr Minimally Invasive Neurosurgery With AI-assisted Robotic guidanCe for Hemorrhagic Stroke

NCT06459427 · tracked via the Priya Life Science China tracker
Sponsor
Yanbing Yu
Phase
Not applicable
Started
2026-05-23
Last updated
2026-09-23

Condition(s) studied

Brain Stem HemorrhageRobotic Surgical Procedures

Investigational drug(s) / intervention(s)

Robot-assisted minimally invasive puncture and aspiration surgeryStandard medical management

Robot-assisted minimally invasive puncture and aspiration surgery: Positioning and surgical operation will be performed according to the robot navigation system protocols. Preoperative imaging data will be used for precise surgical planning, including the construction of a three-dimensional (3D) preoperative visualization model. The 3D reconstruction and CT data will be imported into the AI robot-assisted stereotactic system, which, after mapping to the patient's skull, automatically designs the surgical target, calculates coordinate values, plans the puncture trajectory, and determines the cranial entry point. Different surgical approaches will be selected based on the location and shape of the hematoma, and individualized parameters, including puncture direction and trajectory length, will be generated for each patient. During the procedure, the robot will assist with stereotactic puncture, while the patient's heart rate and blood pressure are closely monitored.

Standard medical management: According to the "Chinese Neurosurgical Expert Consensus on the Diagnosis and Treatment of Primary Brainstem Hemorrhage", conventional medical treatment includes oxygen therapy, specialized nursing care, blood pressure control (maintaining BP at ≤140/90 mmHg), sedation, intracranial pressure reduction, arousal promotion, gastric protection, maintenance of internal homeostasis, infection prevention, neuro-nutrition, brain function support, nutritional support, and overall systemic management; For comatose patients, ensure a patent airway, provide nebulization and sputum clearance, prevent respiratory depression, and improve respiratory function. Closely monitor the patient's condition and provide active symptomatic treatment as needed. Regular cranial CT scans are performed to evaluate intracranial status, and in cases of ventricular hemorrhage or obstructive hydrocephalus, lateral ventricular puncture and drainage may be performed.

Study summary

The purpose of this clinical trial is to observe the improvements in clinical symptoms and imaging outcomes for brainstem hemorrhage using robot-assisted stereotactic puncture, evaluate the clinical efficacy and safety of this treatment, and explore the development of a high-precision, intelligent, and individualized microsurgical diagnosis and treatment process for brainstem hemorrhage. The main questions it aims to address are:

* Establish a multi-center clinical database for brainstem hemorrhage.
* Clinically observe and evaluate the intervention effects of robot-assisted stereotactic puncture on brainstem hemorrhage, compare it with the traditional conservative treatment control group, and investigate its efficacy and impact on patient survival, motor evoked potentials, and the degree of neurological deficits.
* Optimize the Artificial Intelligence (AI) algorithm-based robotic surgical assistance system, and explore the prediction of preoperative brainstem hematoma stability and hematoma path planning.

Participants in the experimental group will:

* Undergo robot-assisted stereotactic minimally invasive surgery for brainstem hematoma puncture
* Receive conservative non-surgical treatment.

If there is a control group: the researchers will compare the conservative non-surgical treatment group to evaluate the effectiveness of robot-assisted stereotactic minimally invasive surgery for brainstem hematoma puncture.

Eligibility

Sex
ALL
Min age
18 Years
Max age
Healthy volunteers
No
Participants must meet all of the following inclusion criteria: 1. Age ≥18 years at randomization; 2. Diagnosed with brainstem hemorrhage via imaging (CT, CTA, etc.); 3. Hematoma volume ≥3 mL; 4. Glasgow Coma Scale (GCS) score of 3-12; 5. Available for surgery within 48 hours after onset; 6. Modified Rankin Scale (mRS) score ≤ 1 prior to this hemorrhage; 7. Informed consent obtained in accordance with national laws, regulations, and applicable ethics committee requirements. Patients will be excluded if they meet any of the following criteria: 1. Hematoma involving other regions such as the supratentorial compartment, basal ganglia, thalamus, midbrain, or ventricles. 2. Radiologically confirmed cerebral vascular abnormalities including ruptured aneurysms, arteriovenous malformations (AVMs), or Moyamoya disease; hemorrhagic transformation of ischemic infarcts; or recent (within 1 year) recurrence of intracerebral hemorrhage; 3. Any irreversible coagulation disorder or known coagulopathy; platelet count \<100,000/µL; INR \>1.4; or use of anticoagulant medication within 7 days before the current hemorrhage; 4. Current or probable pregnancy; 5. Patients with concurrent severe illness likely to influence outcome assessment; 6. Difficulty in follow-up or poor compliance due to any cause.

Primary outcome measure(s)

Trial sites (15)

FacilityCityRegionStatus
China-Japan Friendship Hospital Beijing Beijing Municipality Recruiting
Aerospace Center Hospital Beijing Beijing Municipality Recruiting
The First Affiliated Hospital of Guangxi Medical University Nanning Guangxi Recruiting
Hebei Provincial People's Hospital Shijiazhuang Hebei Recruiting
Nanjing Drum Tower Hospital Nanjing Jiangsu Recruiting
Affiliated Hospital of Nantong University Nantong Jiangsu Recruiting
The Second Affiliated Hospital of Nanchang University Nanchang Jiangxi Recruiting
Huashan Hospital Fudan University Shanghai Shanghai Municipality Recruiting
Shanghai East Hospital, Tongji University Shanghai Shanghai Municipality Recruiting
Shanghai Minhang District Central Hospital Shanghai Shanghai Municipality Recruiting
Jinshan Hospital, Fudan University Shanghai Shanghai Municipality Recruiting
Tianjin Huanhu Hospital Tianjin Tianjin Municipality Recruiting
The Second Affiliated Hospital of Zhejiang University School of Medicine Hangzhou Zhejiang Recruiting
Jinhua Municipal Central Hospital / Jinhua Hospital Affiliated to Zhejiang University School of Medicine Jinhua Zhejiang Recruiting
The First Affiliated Hospital of Wenzhou Medical University Wenzhou Zhejiang Recruiting

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06459427 on ClinicalTrials.gov ↗ ← All trials in China