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NCT Number: NCT07205263

RAINBOW-ICH Trial of AI Guided Minimally Invasive Neurosurgery for ICH

Intracerebral hemorrhage (ICH) is one of the most devastating forms of stroke, with high rates of death and disability worldwide. Despite advances in medical and surgical care, effective therapeutic options remain limited. To address this gap, the RAINBOW-ICH trial has been designed as a nationwide, multicenter, randomized umbrella trial evaluating the efficacy and safety of AI-assisted, robotic-guided minimally invasive neurosurgery compared with conventional strategies across major ICH subtypes.

Under a single master protocol, RAINBOW-ICH incorporates multiple parallel randomized controlled substudies, each targeting a distinct ICH population-large basal ganglia hemorrhage, moderate basal ganglia hemorrhage, intraventricular hemorrhage, and brainstem hemorrhage. This umbrella design allows efficient use of resources while generating high-quality evidence tailored to the specific needs of different ICH subgroups, thereby supporting a more patient-centered approach to care.

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Key information

About this study

Intracerebral hemorrhage (ICH) is a leading cause of stroke-related mortality and long-term disability worldwide. Conventional surgical techniques, including craniotomy and catheter-based drainage, are often associated with significant procedural risks and variable outcomes across clinical settings. Minimally invasive approaches have been proposed to reduce surgical trauma, improve precision, and enhance recovery. Recent studies, such as the ENRICH trial, have provided encouraging evidence that selected patients may benefit from early minimally invasive hematoma evacuation, though results remain heterogeneous and further validation is needed across different ICH subtypes and populations.

The RAINBOW-ICH trial has been established to address this critical gap by systematically evaluating the role of AI-assisted, robotic-guided minimally invasive neurosurgery. Advances in robotics and artificial intelligence have enabled neurosurgeons to achieve greater precision in hematoma evacuation, minimize surgical injury, and improve reproducibility of complex procedures. RAINBOW-ICH is designed as a nationwide, multicenter umbrella trial, conducted under a single master protocol, with multiple parallel randomized controlled substudies. Each substudy focuses on a distinct ICH population and directly compares AI-assisted robotic-guided hematoma evacuation with the conventional standard of care relevant to that subgroup. Specifically, RAINBOW-LBH (NCT06484374) evaluates patients with large basal ganglia hemorrhage, RAINBOW-MBH (NCT06465719) addresses moderate basal ganglia hemorrhage, RAINBOW-IVH (NCT06486480) investigates intraventricular hemorrhage, and RAINBOW-BSH (NCT06459427) targets brainstem hemorrhage.

Within each substudy, participants are randomized to receive either AI-assisted robotic-guided minimally invasive neurosurgery or the control intervention, such as conventional craniotomy, external ventricular drainage, or optimized medical management. All substudies are conducted as multicenter RCTs across China, ensuring adequate and rapid recruitment, generalizability, and rigorous evaluation of interventions in diverse clinical environments.

By integrating minimally invasive neurosurgical technologies with a unified multicenter umbrella trial design, RAINBOW-ICH represents the first large-scale effort in China to rigorously test and compare surgical strategies for ICH. The findings are expected to generate high-quality evidence, refine clinical practice, and ultimately improve neurological outcomes for patients with this devastating disease.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Umbrella Trial Inclusion Criteria:

  • Age ≥18 years;
  • Clinical diagnosis of spontaneous hemorrhagic stroke;

Umbrella Trial Exclusion Criteria:

  • Radiologically diagnosed cerebrovascular abnormalities, as well as ischemic infarction converting to intracerebral hemorrhage, or recent (within 1 year) recurrence of intracerebral hemorrhage;

Each substudy will specify additional inclusion and exclusion criteria in the respective Substudy-specific Registration. Patients who fulfill the overall umbrella trial criteria will be assessed for enrollment into each substudy.

Treatment and study plan

AI-assisted robotic-guided endoscopic hematoma evacuation

Procedure

Surgical removal of hematoma using AI-assisted robotic-guided stereotactic navigation and endoscopic aspiration techniques.

Conventional craniotomy

Procedure

Standard open surgical evacuation of hematoma through craniotomy.

AI-assisted robotic-guided puncture and hematoma evacuation

Procedure

AI-assisted robotic-guided stereotactic puncture and aspiration of hematoma.

Standard medical management

Other

Guideline-based conservative therapy without surgical hematoma evacuation.

AI-assisted robotic-guided endoscopic ventricular hematoma evacuation plus external ventricular drainage

Procedure

AI-assisted robotic-guided endoscopic evacuation of ventricular hematoma combined with external ventricular drainage.

External ventricular drainage (EVD)

Procedure

Conventional ventricular catheter placement for hematoma drainage.

Primary outcomes

  1. Utility-weighted modified Rankin Scale (UW-mRS)

    Time frame: Umbrella level time frame: 6 months; Substudy specific time frame may differ (details will be included in substudy-specific registration)

    The mRS is a 7-level ordinal scale used to evaluate functional outcomes after stroke. The categories are defined as follows:

    0 = No symptoms

    • = No significant disability. Able to carry out all usual activities, despite some symptoms.
    • = Slight disability. Able to look after own affairs without assistance, but unable to carry out all previous activities.
    • = Moderate disability. Requires some help, but able to walk unassisted.
    • = Moderately severe disability. Unable to attend to own bodily needs without assistance, and unable to walk unassisted.
    • = Severe disability. Requires constant nursing care and attention, bedridden, incontinent.
    • = Dead Utility-weighted modified Rankin Scale (UW-mRS) , which applies utility values to each mRS category as shown below: mRS 0= UW-mRS 1;mRS 1= UW-mRS 0.91; mRS 2= UW-mRS 0.76; mRS 3= UW-mRS 0.65; mRS 4= UW-mRS 0.33; mRS 5= UW-mRS 0; mRS 6= UW-mRS 0.

Secondary outcomes

  1. Ordinal shift in modified Rankin Scale

    Time frame: Umbrella level time frame: 6 months; Substudy specific time frame may differ (details will be included in substudy-specific registration)

    Ordinal shift analysis of the modified Rankin Scale (mRS), which measures the degree of disability or dependence in daily activities after stroke. The scale ranges from 0 (no symptoms) to 6 (death). This outcome assesses whether there is a shift toward better or worse functional status across the full ordinal distribution of mRS scores.

  2. Excellent functional neurological outcome

    Time frame: Umbrella level time frame: 6 months; Substudy specific time frame may differ (details will be included in substudy-specific registration)

    Excellent functional neurological outcome means modified Rankin scale (mRS) scores 0-1. The minimum mRS is 0 (no symptoms) while the maximum mRS is 6 (death). The higher the mRS score is the worse outcome is.

  3. Independent functional neurological outcome

    Time frame: Umbrella level time frame: 6 months; Substudy specific time frame may differ (details will be included in substudy-specific registration)

    Independent functional neurological outcome means modified Rankin scale (mRS) scores 0-2. The minimum mRS is 0 (no symptoms) while the maximum mRS is 6 (death). The higher the mRS score is the worse outcome is.

  4. Health Related Quality of Life

    Time frame: Umbrella level time frame: 6 months; Substudy specific time frame may differ (details will be included in substudy-specific registration)

    Health Related Quality of Life based on EuroQol 5 Dimension 5 Level (EQ-5D-5L).The EQ-5D-5L is a generic instrument for describing and valuing health. It assesses five domains: Mobility, Self-Care, Usual Activities, Pain/Discomfort, and Anxiety/Depression. Each dimension has five response categories corresponding to: no problems, slight, moderate, severe and extreme problems.

  5. Total length of hospital stay

    Time frame: Umbrella level time frame: 6 months; Substudy specific time frame may differ (details will be included in substudy-specific registration)

    Total length of hospital stay refers to the number of days from the date of hospital admission to the date of discharge.

Other outcomes

  1. Mortality

    Time frame: Umbrella level time frame: 6 months; Substudy specific time frame may differ (details will be included in substudy-specific registration)

    Mortality status equals to death which will be collected at all visits during the trial period

Study contacts

Contact information is provided by the study sponsor or research team.

Gao Chen, MD.

CONTACT

[email protected]

+86 0571 87784813

Xiaobo Yu, MD.

CONTACT

[email protected]

+86 0571 87784816

Sponsors and collaborators

Lead sponsor

Second Affiliated Hospital, School of Medicine, Zhejiang University

Other

Collaborators

  • China-Japan Friendship Hospital
  • Huashan Hospital
  • The Affiliated Nanjing Drum Tower Hospital of Nanjing University Medical School

Registry information

Official study title

A Multicenter, Randomized, Controlled, Umbrella Trial for Minimally Invasive Neurosurgery With Al-assisted Robotic Guidance for Hemorrhagic Stroke (RAINBOW-ICH)

Acronym: RAINBOW-ICH

Important dates

Study start
2025
Primary completion
2027
Study completion
2027
First posted
Oct 3, 2025
Registry last updated
Jan 8, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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