Use of Tissue Plasminogen Activator in the Clearance of Chronic Subdural Hematomas
Primary Purpose
Hematoma, Subdural, Fibrinolytic; Hemorrhage
Status
Recruiting
Phase
Phase 4
Locations
Canada
Study Type
Interventional
Intervention
Tissue Plasminogen Activator
Placebo
Sponsored by
About this trial
This is an interventional treatment trial for Hematoma, Subdural
Eligibility Criteria
Inclusion Criteria:
- Adult patients (18 yrs or older)
- Admitted to neurosurgery wing at the hospital
- Symptomatic patients requiring surgical drainage by twist drill craniostomy
Exclusion Criteria:
- Patients at increased risk of bleeding such as patients taking anticoagulation medication that required reversal at time of intervention، or those with coagulopathic disorder.
- Patients on antiplatelets or anticoagulation medications (DOACs or warfarin) with appropriate holding period prior to drainage, those who are eventually minimized to a regular bleeding risk compared to the normal population, will be included in the study.
- Patients with subdural empyema.
- Redo twist drill craniostomy for residual cSDH within the same admission.
- Drain accidentally removed during nursing care or patient transport before 24 hr interval scan.
- Patients who are not expected to live more than three months.
Sites / Locations
- Hamilton General HospitalRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Placebo Comparator
Arm Label
Intervention - tPA administered
Placebo Control
Arm Description
This group will receive 2mL of intra-catheter tPA during twist drill craniostomy procedure
This group will receive 2mL of intra-catheter saline solution during twist drill craniostomy procedure
Outcomes
Primary Outcome Measures
Study Feasibility
Patient recruitment rate, eligibility of patients, protocol adherence, unexpected events
Secondary Outcome Measures
Reoperation rate
Reoperation rate in the first 6 weeks post drainage
Volume of chronic subdural hematoma
Volume, as measured in 3 intervals: pre-procedure, post-procedure at 24hrs and 6 weeks
Rate of adverse events
Rate of adverse events in the first 6 weeks post procedure, including CNS infection, seizure, post-op hemorrhage
Length of hospital stay
length of hospital stay in days
Full Information
NCT ID
NCT05491356
First Posted
August 4, 2022
Last Updated
September 21, 2023
Sponsor
Hamilton Health Sciences Corporation
1. Study Identification
Unique Protocol Identification Number
NCT05491356
Brief Title
Use of Tissue Plasminogen Activator in the Clearance of Chronic Subdural Hematomas
Official Title
The Utility of Intra-Catheter Fibrinolytics in Draining Chronic Subdural Hematomas: A Randomized Controlled Trial Pilot Study
Study Type
Interventional
2. Study Status
Record Verification Date
September 2023
Overall Recruitment Status
Recruiting
Study Start Date
May 11, 2023 (Actual)
Primary Completion Date
January 2024 (Anticipated)
Study Completion Date
March 2024 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Hamilton Health Sciences Corporation
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
To determine the utility of tissue plasminogen activator (tPA) in the clearance of chronic subdural hematomas (CSDH). Intra-catheter tPA will be administered during surgical procedure and allowed to break down blood clot to assist with removal/drainage during twist drill craniostomy procedure.
Detailed Description
A chronic subdural hematoma (CSDH) is a collection of blood overlying the brain that can be seen, usually in the elderly with even minimal head trauma. These are usually treated by removing the collection of blood. This can be done through a small drill hole in the skull or by larger holes (one or two) the size of a nickel. Sometimes a larger piece of skull is removed to be able to remove the CSDH. The standard practice at our center is to do these procedures under local anesthesia with a twist drill craniostomy (small drill hole through the skull). In some cases, all the CSDH can not be removed the first time, requiring a second procedure or a larger procedure. This study plans to use a type of medication that breaks down the solid blood clot, enabling more of it to drain. This medication (tpa) is already used in other surgeries and is safe to use in humans. Our preliminary experience and that of others suggests very low risk at the dosages being used. We hope that using this new drug will decrease the chance of the CSDH collecting again and reduce the overall length of your stay in the hospital and reduce the need for further surgery.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hematoma, Subdural, Fibrinolytic; Hemorrhage
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Single Group Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
40 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Intervention - tPA administered
Arm Type
Experimental
Arm Description
This group will receive 2mL of intra-catheter tPA during twist drill craniostomy procedure
Arm Title
Placebo Control
Arm Type
Placebo Comparator
Arm Description
This group will receive 2mL of intra-catheter saline solution during twist drill craniostomy procedure
Intervention Type
Drug
Intervention Name(s)
Tissue Plasminogen Activator
Intervention Description
Dosage of 1mg/mL mixed in 0.9% saline solution, intra-catheter administration, sterile
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
0.9% saline solution, intra-catheter administration, sterile
Primary Outcome Measure Information:
Title
Study Feasibility
Description
Patient recruitment rate, eligibility of patients, protocol adherence, unexpected events
Time Frame
8 months
Secondary Outcome Measure Information:
Title
Reoperation rate
Description
Reoperation rate in the first 6 weeks post drainage
Time Frame
8 months
Title
Volume of chronic subdural hematoma
Description
Volume, as measured in 3 intervals: pre-procedure, post-procedure at 24hrs and 6 weeks
Time Frame
8 months
Title
Rate of adverse events
Description
Rate of adverse events in the first 6 weeks post procedure, including CNS infection, seizure, post-op hemorrhage
Time Frame
8 months
Title
Length of hospital stay
Description
length of hospital stay in days
Time Frame
8 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
100 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Adult patients (18 yrs or older)
Admitted to neurosurgery wing at the hospital
Symptomatic patients requiring surgical drainage by twist drill craniostomy
Exclusion Criteria:
Patients at increased risk of bleeding such as patients taking anticoagulation medication that required reversal at time of intervention، or those with coagulopathic disorder.
Patients on antiplatelets or anticoagulation medications (DOACs or warfarin) with appropriate holding period prior to drainage, those who are eventually minimized to a regular bleeding risk compared to the normal population, will be included in the study.
Patients with subdural empyema.
Redo twist drill craniostomy for residual cSDH within the same admission.
Drain accidentally removed during nursing care or patient transport before 24 hr interval scan.
Patients who are not expected to live more than three months.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Dr. Kesava Reddy
Phone
905-521-0061
Email
reddy@hhsc.ca
First Name & Middle Initial & Last Name or Official Title & Degree
Jessy Moore, MSc
Phone
289-686-8827
Email
moorej@hhsc.ca
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Dr. Kesava Reddy
Organizational Affiliation
Hamilton Health Sciences Corporation
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hamilton General Hospital
City
Hamilton
State/Province
Ontario
ZIP/Postal Code
L8L 2X2
Country
Canada
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Dr. Kesava Reddy
Phone
905-521-2100
Email
reddy@hhsc.ca
First Name & Middle Initial & Last Name & Degree
Jessy Moore
Phone
289-686-8827
Email
moorej@hhsc.ca
First Name & Middle Initial & Last Name & Degree
Dr. Kesava Reddy
First Name & Middle Initial & Last Name & Degree
Dr. Mohamed Alhantoobi
12. IPD Sharing Statement
Plan to Share IPD
Undecided
IPD Sharing Plan Description
Patient data will be de-identified and the data will be analyzed as a whole before becoming available to other researchers.
De-identified IPD may be shared with other researchers if necessary based on occurrence of adverse events occurrence, circumstantial findings, etc.
Citations:
PubMed Identifier
22120294
Citation
Neils DM, Singanallur PS, Wang H, Tracy P, Klopfenstein J, Dinh D, Elwood PW, Fassett D, McCall T, Lin J, Tsung A. Recurrence-free chronic subdural hematomas: a retrospective analysis of the instillation of tissue plasminogen activator in addition to twist drill or burr hole drainage in the treatment of chronic subdural hematomas. World Neurosurg. 2012 Jul;78(1-2):145-9. doi: 10.1016/j.wneu.2011.08.032. Epub 2011 Nov 7.
Results Reference
background
PubMed Identifier
32025399
Citation
Brazdzionis J, Patchana T, Wiginton JG 4th, Wacker MR, Menoni R, Miulli DE. Intracatheter Tissue Plasminogen Activator for Chronic Subdural Hematomas after Failed Bedside Twist Drill Craniostomy: A Retrospective Review. Cureus. 2019 Dec 26;11(12):e6472. doi: 10.7759/cureus.6472.
Results Reference
background
PubMed Identifier
33722722
Citation
O YM, Tsang SL, Leung GK. Fibrinolytic-Facilitated Chronic Subdural Hematoma Drainage-A Systematic Review. World Neurosurg. 2021 Jun;150:e408-e419. doi: 10.1016/j.wneu.2021.03.029. Epub 2021 Mar 17.
Results Reference
background
Learn more about this trial
Use of Tissue Plasminogen Activator in the Clearance of Chronic Subdural Hematomas
We'll reach out to this number within 24 hrs