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Sealant Patch
Sealant Patch for Cerebrospinal Fluid Leak (ENCASE-II Trial)
N/A
Waitlist Available
Research Sponsored by Polyganics BV
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up up to 5 years
Awards & highlights
No Placebo-Only Group
Summary
This trial is testing LIQOSEAL®, a product that helps seal brain surgery sites to prevent fluid leaks, in patients having elective brain surgery. It works like a patch to stop brain fluid from escaping through the surgical wound.
Who is the study for?
This trial is for adults over 18 who can consent and follow the study plan. Women must use birth control if they can have children. Participants need a clean surgical wound and at least 5mm of dural space around the opening. Excluded are those with certain dural diseases, MRI issues, high infection risk, recent other trials participation, large dural openings, LIQOSEAL® history or allergies to it.
What is being tested?
The trial tests LIQOSEAL®'s ability to prevent cerebrospinal fluid (CSF) leaks after brain surgery compared to DuraSeal and Adherus. It aims to show that LIQOSEAL® is not worse than the controls in stopping CSF leaks post-operation.
What are the potential side effects?
While specific side effects aren't listed here, potential risks may include allergic reactions to patch components, complications from improper sealing leading to CSF leakage which could result in headaches or infections.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ up to 5 years
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~up to 5 years
Treatment Details
Awards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: Investigational armExperimental Treatment1 Intervention
Application of LIQOSEAL after closure of dura mater
Group II: Control armActive Control1 Intervention
Application of Adherus or DurSeal after closure of dura mater
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
LIQOSEAL
2021
N/A
~230
Research Highlights
Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
The most common treatments for cerebrospinal fluid (CSF) leaks involve the use of dural sealants, such as LIQOSEAL®, which work by creating a watertight seal over the dural closure to prevent CSF leakage. These sealants typically contain biocompatible materials that adhere to the tissue and promote healing.
The mechanism of action is crucial for CSF leak patients as it directly addresses the primary issue of preventing fluid escape, thereby reducing the risk of complications such as infections and promoting faster recovery. Effective sealing of the dura mater ensures that the integrity of the central nervous system is maintained, which is essential for patient outcomes.
The Antiedematous Effect of Exogenous Lactate Therapy in Traumatic Brain Injury: A Physiological and Mechanistic Approach.Comparison of equivolume, equiosmolar solutions of mannitol and hypertonic saline with or without furosemide on brain water content in normal rats.Causes of arachnoid cyst development and expansion.
The Antiedematous Effect of Exogenous Lactate Therapy in Traumatic Brain Injury: A Physiological and Mechanistic Approach.Comparison of equivolume, equiosmolar solutions of mannitol and hypertonic saline with or without furosemide on brain water content in normal rats.Causes of arachnoid cyst development and expansion.
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Who is running the clinical trial?
Polyganics BVLead Sponsor
5 Previous Clinical Trials
223 Total Patients Enrolled
1 Trials studying Cerebrospinal Fluid Leak
40 Patients Enrolled for Cerebrospinal Fluid Leak
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- You have any kind of disease in the area where the dura will be closed.You are 18 years old or older.You cannot have an MRI for medical reasons.You are at risk of being harmed by an increase in PEEP (positive end-expiratory pressure).You are suspected to have an infection that needs antibiotics.You need to have another surgery in the same area within 90 days.The size of the opening in the protective covering of the brain is larger than the size of the patch that can be used to cover it.People who have used LIQOSEAL® before.You will need surgery that involves placing devices or draining fluid from inside your brain.You have had a type of surgery where a specific material was used to close the covering of the brain, called the dura mater.You have a gap in the protective layer around your brain that is larger than 3 mm after it has been closed.You need to have at least 5 mm of space around the dural opening in your body.You have an allergy to any parts of LIQOSEAL®.You don't have any leaking of cerebrospinal fluid after surgery and your PEEP is normal.You have a condition that affects your blood's ability to clot due to medication or other reasons.You have hydrocephalus.
Research Study Groups:
This trial has the following groups:- Group 1: Control arm
- Group 2: Investigational arm
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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