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Stereotactic, Robot-assisted Intracerebral Hemorrhage Clot Evacuation

Primary Purpose

Intracerebral Hematoma

Status
Withdrawn
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Intracerebral catheter placement
Robot-assisted intracerebral catheter
Sponsored by
Zimmer Biomet
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Intracerebral Hematoma

Eligibility Criteria

18 Years - 85 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Age 18-85
  • Head CT demonstrates an acute, spontaneous, supratentorial, primary ICH
  • ICH volume ≥30 cc
  • Surgery initiated within 48 hours of hospital admission

Exclusion Criteria:

  • Pregnancy at the time of surgery
  • Underlying vascular lesion defined as causative source of ICH
  • Irreversible coagulopathy
  • Profound neurological deficit defined as fixed/dilated pupils, bilateral extensor motor posturing
  • Infratentorial or brainstem ICH
  • Known life expectancy <6 months

Sites / Locations

  • UPMC Stroke Institute

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Intracerebral hemorrhage

Arm Description

Patients with ICH meeting inclusion/exclusion criteria undergo ROSA stereotactic robot-assisted intracerebral catheter placement to evacuate intracerebral or intracranial hemorrhage

Outcomes

Primary Outcome Measures

Hematoma volume reduction
Percentage of hematoma evacuation identified by CT scan

Secondary Outcome Measures

Linear measurement of accuracy
Accuracy of catheter placement is assessed by comparing planned stereotactic trajectories to actual location of the intracerebral catheter. Measure of linear displacement is given in millimeters.
Functional Outcomes measured by modified Rankin Scale (mRS) for neurologic disabilities
mRS evaluates in a scale 0-6 the degree of disability in patients who have suffered a cerebral stroke or hemorrhage.

Full Information

First Posted
January 16, 2018
Last Updated
July 16, 2021
Sponsor
Zimmer Biomet
Collaborators
University of Pittsburgh Medical Center
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1. Study Identification

Unique Protocol Identification Number
NCT03414307
Brief Title
Stereotactic, Robot-assisted Intracerebral Hemorrhage Clot Evacuation
Official Title
ROSA Stereotactic Robot-assisted Intracerebral Hemorrhage Clot Evacuation
Study Type
Interventional

2. Study Status

Record Verification Date
July 2021
Overall Recruitment Status
Withdrawn
Why Stopped
COVID 19 Pandemic
Study Start Date
September 30, 2020 (Actual)
Primary Completion Date
September 30, 2020 (Actual)
Study Completion Date
September 30, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Zimmer Biomet
Collaborators
University of Pittsburgh Medical Center

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
Yes
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Non-traumatic intracerebral hemorrhage (ICH) affects approximately 100,000 Americans yearly. Up to 30-50% of ICH is fatal, and those patients who survive are often left with significant neurologic dysfunction. In the past, medical management (e.g., control of hypertension, reversal of antiplatelet or anticoagulants) had been the most effective treatment for these patients, given the morbidity and mortality associated with open surgical treatment for evacuation of ICH. However, recent trials have demonstrated that minimally invasive stereotactic neurosurgical procedures to evacuate ICH are safe and result in improved outcomes for these patients. Initial attempts to evaluate the efficacy of surgical evacuation of ICH found no significant difference between medical management and standard craniotomy for surgical evacuation. Indeed, open surgery was often discouraged for these patients due to the significant morbidity and mortality associated with the surgical procedure itself. However, research has demonstrated that minimally invasive, image guided stereotactic frame-based and frameless methods are effective and safe for the placement of catheters for clot aspiration and fibrinolytic therapy of ICH in the basal ganglia and other deep seated regions. Larger randomized controlled trials have demonstrated that these minimally invasive approaches also offer clinical benefit for these patients.
Detailed Description
The introduction of the ROSA stereotactic robot offers an image guided stereotactic approach with greater precision and accuracy than traditional frame-based and frameless methods. While the ROSA has never been used for the placement of intra-hemorrhage catheters, prior applications such as brain biopsies and abscess drainage represent similar surgical procedures which require the same planning, precision, and surgical technique. At the very least, ROSA offers an accurate image guided approach to deep lesions that should be comparable to competitive image guided platforms. At best, ROSA offers superior trajectory planning software, greater ease in planning multiple trajectories to large, irregular clots, and the potential for robot aided navigation into and out of the hematoma which is the greatest source of human error in these cases. For instance, the procedure often requires advancement of a larger aspiration catheter, slow aspiration as the catheter is withdrawn, and then re-advancement of a smaller catheter into the hematoma, which is left in place. The ability to advance and remove catheters in a fixed trajectory with robotic assistance may represent the greatest advantage of ROSA.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Intracerebral Hematoma

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
Subject enrolled serve as their own control to evaluate the effect of ROSA robotic-assisted intracerebral catheter placement.
Masking
None (Open Label)
Allocation
N/A
Enrollment
0 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Intracerebral hemorrhage
Arm Type
Experimental
Arm Description
Patients with ICH meeting inclusion/exclusion criteria undergo ROSA stereotactic robot-assisted intracerebral catheter placement to evacuate intracerebral or intracranial hemorrhage
Intervention Type
Procedure
Intervention Name(s)
Intracerebral catheter placement
Other Intervention Name(s)
Stereotactic catheter placement
Intervention Description
Image guided stereotactic placement of intra-hemorrhage catheters to evacuate intra-cerebral hemorrhage
Intervention Type
Device
Intervention Name(s)
Robot-assisted intracerebral catheter
Other Intervention Name(s)
ROSA
Intervention Description
ROSA is a robotic device with trajectory planning software that can be used to aid in planning multiple trajectories to large, irregular clots, and aids in navigating into and out of the cerebral hematoma with minimum human error.
Primary Outcome Measure Information:
Title
Hematoma volume reduction
Description
Percentage of hematoma evacuation identified by CT scan
Time Frame
Day 1 to Day 4 post operative
Secondary Outcome Measure Information:
Title
Linear measurement of accuracy
Description
Accuracy of catheter placement is assessed by comparing planned stereotactic trajectories to actual location of the intracerebral catheter. Measure of linear displacement is given in millimeters.
Time Frame
Day 0
Title
Functional Outcomes measured by modified Rankin Scale (mRS) for neurologic disabilities
Description
mRS evaluates in a scale 0-6 the degree of disability in patients who have suffered a cerebral stroke or hemorrhage.
Time Frame
Baseline, 3-month, 6-month and 1-year post-operative

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
85 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age 18-85 Head CT demonstrates an acute, spontaneous, supratentorial, primary ICH ICH volume ≥30 cc Surgery initiated within 48 hours of hospital admission Exclusion Criteria: Pregnancy at the time of surgery Underlying vascular lesion defined as causative source of ICH Irreversible coagulopathy Profound neurological deficit defined as fixed/dilated pupils, bilateral extensor motor posturing Infratentorial or brainstem ICH Known life expectancy <6 months
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Oscar Gonzalez, MD, DNP
Organizational Affiliation
Zimmer Biomet
Official's Role
Study Chair
Facility Information:
Facility Name
UPMC Stroke Institute
City
Pittsburgh
State/Province
Pennsylvania
ZIP/Postal Code
15213
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
27751554
Citation
Hanley DF, Thompson RE, Muschelli J, Rosenblum M, McBee N, Lane K, Bistran-Hall AJ, Mayo SW, Keyl P, Gandhi D, Morgan TC, Ullman N, Mould WA, Carhuapoma JR, Kase C, Ziai W, Thompson CB, Yenokyan G, Huang E, Broaddus WC, Graham RS, Aldrich EF, Dodd R, Wijman C, Caron JL, Huang J, Camarata P, Mendelow AD, Gregson B, Janis S, Vespa P, Martin N, Awad I, Zuccarello M; MISTIE Investigators. Safety and efficacy of minimally invasive surgery plus alteplase in intracerebral haemorrhage evacuation (MISTIE): a randomised, controlled, open-label, phase 2 trial. Lancet Neurol. 2016 Nov;15(12):1228-1237. doi: 10.1016/S1474-4422(16)30234-4. Epub 2016 Oct 11.
Results Reference
result
PubMed Identifier
27758940
Citation
Vespa P, Hanley D, Betz J, Hoffer A, Engh J, Carter R, Nakaji P, Ogilvy C, Jallo J, Selman W, Bistran-Hall A, Lane K, McBee N, Saver J, Thompson RE, Martin N; ICES Investigators. ICES (Intraoperative Stereotactic Computed Tomography-Guided Endoscopic Surgery) for Brain Hemorrhage: A Multicenter Randomized Controlled Trial. Stroke. 2016 Nov;47(11):2749-2755. doi: 10.1161/STROKEAHA.116.013837. Epub 2016 Oct 6. Erratum In: Stroke. 2017 Nov;48(11):e335.
Results Reference
result
PubMed Identifier
23726393
Citation
Mendelow AD, Gregson BA, Rowan EN, Murray GD, Gholkar A, Mitchell PM; STICH II Investigators. Early surgery versus initial conservative treatment in patients with spontaneous supratentorial lobar intracerebral haematomas (STICH II): a randomised trial. Lancet. 2013 Aug 3;382(9890):397-408. doi: 10.1016/S0140-6736(13)60986-1. Epub 2013 May 29. Erratum In: Lancet. 2013 Aug 3;382(9890):396. Lancet. 2021 Sep 18;398(10305):1042.
Results Reference
result
PubMed Identifier
17674294
Citation
Kim IS, Son BC, Lee SW, Sung JH, Hong JT. Comparison of frame-based and frameless stereotactic hematoma puncture and subsequent fibrinolytic therapy for the treatment of supratentorial deep seated spontaneous intracerebral hemorrhage. Minim Invasive Neurosurg. 2007 Apr;50(2):86-90. doi: 10.1055/s-2007-982503.
Results Reference
result

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Stereotactic, Robot-assisted Intracerebral Hemorrhage Clot Evacuation

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