MIECH: The Minimally Invasive Endoscopic Surgery With the Axonpen System for Spontaneous Intracerebral Hemorrhage

Intracerebral Hemorrhage Clinical Trial

Official title:

The Minimally Invasive Endoscopic Surgery With the Axonpen System for Spontaneous Intracerebral Hemorrhage (MIECH): An Open-label, Non-randomized, Single-arm Pilot Study

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04839770
• Other study ID #: MIECH-2020-01
• Status: Completed
• Phase: N/A
• Start date: August 7, 2020
• Est. completion date: January 31, 2023

Study information

• Verified date: March 2023
• Source: Clearmind Biomedical Inc.
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The primary objective of this trial is to provide preliminary safety data of minimally invasive endoscopic surgery using the Axonpen™ system for spontaneous intracerebral hemorrhage (ICH). The effectiveness of the Axonpen™ system in early hematoma removal and the surgical impact on subject's functional recovery will also be evaluated. The Axonpen™ system, consisting of a neuroendoscope (Axonpen) and a monitor (Axonmonitor), is cleared by FDA and indicated for the illumination and visualization of intracranial tissue and fluids and the controlled aspiration of tissue and/or fluid during surgery of the ventricular system or cerebrum.

Description:

In the present trial, the FDA-cleared Axonpen™ system was applied on the ICH surgery. The Axonpen™ System is a neuroendoscope combined with the functions of hematoma aspiration and irrigation, aiming to minimize surgical brain injury, optimize surgical procedure, and be available for early hematoma evacuation. The technique of minimally invasive endoscopic neurosurgery for ICH is still considered in development; however, a retrospective study [Kuo et al.] has shown that early and complete evacuation of ICH may lead to improved outcomes in selected patients, where the neurosurgeons utilized combination of the existing instruments, such as a rod-lens endoscope with irrigation system and a suction coagulator, to enable visualization, aspiration, and irrigation of the hematoma to be worked simultaneously. The technology employed and the results revealed in the previous study provide a proof of concept for the Axonpen™ system, and also imply that the current device could be safe and effective in the management of ICH.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 10
• Est. completion date: January 31, 2023
• Est. primary completion date: October 31, 2022
• Accepts healthy volunteers: No
• Gender: All
• Age group: 20 Years to 80 Years

Eligibility

Inclusion Criteria:

Patients who fulfill ALL the inclusion criteria will be enrolled:

1. Age 20-80 years, all genders/sexes are inclusive;

2. Evidence of a spontaneous basal ganglia ICH on CT scan;

3. Patient, or a family member with legally authorized responsibility, has given informed consent;

4. GCS of 6-14;

5. Volume of hematoma in range of 30-80 ml as measured by the ABC/2 method;

6. Can receive surgical treatment within 48 hours after ictus. Exclusion Criteria:

Patients who fulfill ANY ONE of the exclusion criteria should not be enrolled:

1. Previous symptomatic stroke with neurological sequelae (per history or as seen on initial CT scan);

2. ICH known or suspected by study investigator to be secondary to aneurysm, vascular malformation, hemorrhagic transformation of ischemic stroke, cerebral venous thrombosis, thrombolytic therapy, tumor, or infection;

3. Acute or active infection signs requiring treatment at the time of admission;

4. Significant ventricular extension of the hemorrhage; more than 30 mL of intraventricular hemorrhage;

5. Refractory elevated ICP after placement of an EVD (external ventricular drain);

6. Severe pre-existing physical or mental disability or severe co-morbidity which might interfere with assessment of outcome;

7. Minimally invasive neurosurgery could not be commenced within 48 hours of onset. The case shall be excluded when the time of onset cannot be estimated and is judged with controversy by the investigator;

8. The hematological effects of any previous anticoagulants are not completely reversed (platelet count < 100 × 10^3/µL; international normalized ratio (INR) > 1.4);

9. Hereditary or acquired hemorrhagic diathesis or coagulation factor deficiency;

10. Any condition that could impose hazards to the patient with the MIN or affect the participation of the patient in the study. The judgment is left to the discretion of the investigator;

11. Major surgery within the preceding 14 days which poses risk in the opinion of the investigator;

12. Any history or current evidence suggestive of venous or arterial thrombotic events within the previous 12 months, including clinical, ECG, laboratory, or imaging findings;

13. Use of heparin, low-molecular weight heparin, GPIIb/IIIa antagonist, antiplatelet agents, or oral anticoagulation (e.g., warfarin, factor Xa inhibitor, thrombin inhibitor) within the previous 14 days, irrespective of laboratory values;

14. Pregnancy, breast-feeding, or positive pregnancy test (either serum or urine) (Woman of child-bearing potential must have a negative pregnancy test prior to the study procedure.);

15. Participation in any investigational study in the last 30 days;

16. Known terminal illness or planned withdrawal of care or comfort care measures.

Related Conditions & MeSH terms

• Basal Ganglia Hemorrhage
• Cerebral Hemorrhage
• Hemorrhage
• Intracerebral Hemorrhage
• Intracranial Hemorrhage
• Intracranial Hemorrhages

Intervention

Device:
• Axonpen system
The Axonpen™ system, containing the Axonpen and the Axonmonitor, has been cleared for the illumination and visualization of intracranial tissue and fluids and the controlled aspiration of tissue and/or fluid during surgery of the ventricular system or cerebrum. The Axonpen is a neuroendoscope integrated with suction (sourced from hospital vacuum) and irrigation (sourced from third-party saline infusion bag) functions. The Axonmonitor is used for view and storage of the endoscopic image. The Axonpen™ system is intended to optimize the procedure of minimally invasive neurosurgery for early ICH evacuation.

Locations

Country	Name	City	State
Taiwan	Chang Gung Memorial Hospital (Linkou Branch)	Taoyuan

Sponsors (2)

Lead Sponsor	Collaborator
Clearmind Biomedical Inc.	Chang Gung Memorial Hospital

Country where clinical trial is conducted

Taiwan, 

References & Publications (1)

Kuo LT, Chen CM, Li CH, Tsai JC, Chiu HC, Liu LC, Tu YK, Huang AP. Early endoscope-assisted hematoma evacuation in patients with supratentorial intracerebral hemorrhage: case selection, surgical technique, and long-term results. Neurosurg Focus. 2011 Apr;30(4):E9. doi: 10.3171/2011.2.FOCUS10313. — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Rate of Mortality	Safety will be assessed by determining mortality within 30 days post-operation for all subjects	30 days
Primary	Number of Adverse events (AEs), Serious Adverse Events (SAEs), and Unanticipated Device Effects (UDEs)	AEs, SAEs, and UDEs will be observed from the beginning of the surgery until the last follow-up visit (Day 180) for safety monitoring, and their relation to the study device will be analyzed	180 days
Secondary	Hemorrhage volume	Residual hematoma will be measured via 6 & 72 hours post-operation CT. Reduction (%) of hemorrhage volume will be assessed by comparing with pre-operation CT	6 and 72 hours
Secondary	Glasgow Coma Scale (GCS)	Clinical assessment for level of consciousness and responsiveness before and after surgery (Assessed by the sum of E/V/M scores. E: Eye opening, 1 = None - 4 = Spontaneous. V: Verbal response, 1 = None - 5 = Normal conversation. M: Motor response, 1 = None - 6 = Normal)	180 days
Secondary	modified Rankin Scale (mRS)	Functional outcomes will be measured via mRS at 72 hours and 7 days post-operation, hospital discharge, and 40, 90, 180 days follow-up visits (Scale ranges from 1 to 7, 1 = No symptoms - 7 = Dead)	180 days
Secondary	Glasgow Outcome Scale Extended (GOSE)	Functional outcomes will be measured via GOSE at 72 hours and 7 days post-operation, hospital discharge, and 40, 90, 180 days follow-up visits (Scale ranges from 1 to 8, 1 = Death - 8 = Upper good recovery)	180 days
Secondary	Length of ICU	Duration of stay in the ICU	Number of days from admission, up to 180 days
Secondary	Length of hospitalization	Duration of stay in the hospital	Number of days from admission to discharge, up to 180 days