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Enzyme
Hyaluronidase for Muscle Spasms
Phase 2
Recruiting
Led By Pablo Celnik, MD
Research Sponsored by Johns Hopkins University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Lack of full passive and active range of motion in at least 2/4 areas (shoulder, elbow, forearm, wrist) in the hemiparetic upper limb
Be older than 18 years old
Must not have
Other neurologic condition that may affect motor response (e.g., Parkinson's disease, ALS, MS)
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 9 weeks
Summary
This trial tests if using a special enzyme can help people who have stiff arm muscles after a stroke. The enzyme works by reducing substances that cause muscle tightness, which may improve arm movement and strength. This new therapy aims to reduce muscle stiffness by breaking down certain substances in the muscles.
Who is the study for?
This trial is for individuals who had a stroke 6-120 months ago and are experiencing moderate to severe muscle stiffness in their upper limb. They must be able to consent, undergo MRI scans, and follow the study's procedures. Excluded are those with recent spasticity treatments, other neurological conditions like Parkinson's or ALS, significant cognitive issues or depression, pregnancy, hyaluronidase allergy, claustrophobia or MRI contraindications.
What is being tested?
The trial tests human recombinant hyaluronidase injections against saline (placebo) in reducing muscle stiffness post-stroke. It's double-blind and placebo-controlled with two phases ensuring all participants receive treatment at some point over nine weeks with seven visits including MRIs before the first injection but not after the second.
What are the potential side effects?
Potential side effects may include allergic reactions to hyaluronidase such as swelling or itching at the injection site. Since it’s a blinded study involving placebos as well, distinguishing between actual drug side effects from placebo will be part of the evaluation.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
I can't fully move at least two parts of my arm on one side.
Exclusion Criteria
You may be eligible for the trial if you check “No” for criteria below:Select...
I have a neurological condition like Parkinson's, ALS, or MS.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 9 weeks
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~9 weeks
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Total upper limb passive range of motion
Secondary study objectives
Change in Wolf-Motor Function Test (WMFT) Score
Change in upper limb Fugl-Meyer Assessment Score
Total upper limb active range of motion
Trial Design
2Treatment groups
Experimental Treatment
Placebo Group
Group I: Treatment ArmExperimental Treatment1 Intervention
Hyaluronidase plus saline
Group II: Control ArmPlacebo Group1 Intervention
Normal Saline
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Hyaluronidase
2007
Completed Phase 4
~370
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
Common treatments for muscle spasms include human recombinant hyaluronidase, which breaks down hyaluronic acid to reduce tissue viscosity and muscle stiffness, and botulinum toxin A (BoNT-A), which inhibits acetylcholine release at the neuromuscular junction to relax muscles. Low-Intensity Focused Ultrasound (LIFU) also helps by increasing the expression of neuronal K-Cl cotransporters, reducing muscle hyperactivity.
These treatments are important for muscle spasm patients as they address the root causes of muscle stiffness and hyperactivity, offering relief and enhancing mobility and quality of life.
Low-Intensity Focused Ultrasound Alleviates Spasticity and Increases Expression of the Neuronal K-Cl Cotransporter in the L4-L5 Sections of Rats Following Spinal Cord Injury.Effects of muscle relaxants on ischaemia damage in skeletal muscle.Identification of the optimal dose and calpain system regulation of tetramethylpyrazine on the prevention of skeletal muscle atrophy in hindlimb unloading rats.
Low-Intensity Focused Ultrasound Alleviates Spasticity and Increases Expression of the Neuronal K-Cl Cotransporter in the L4-L5 Sections of Rats Following Spinal Cord Injury.Effects of muscle relaxants on ischaemia damage in skeletal muscle.Identification of the optimal dose and calpain system regulation of tetramethylpyrazine on the prevention of skeletal muscle atrophy in hindlimb unloading rats.
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Who is running the clinical trial?
Johns Hopkins UniversityLead Sponsor
2,323 Previous Clinical Trials
14,874,250 Total Patients Enrolled
Pablo Celnik, MDPrincipal InvestigatorJohns Hopkins University
Ning Cao, MDPrincipal InvestigatorJohns Hopkins University
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- I've had treatments for muscle stiffness in the last year.I had a stroke between 4 months and 15 years ago.I experience significant muscle stiffness.I have a neurological condition like Parkinson's, ALS, or MS.You are willing to have an MRI, complete all clinical assessments, and comply with study protocols.I had a stroke between 6 months and 10 years ago.I had a stroke between 6 months and 10 years ago and have moderately-severe muscle stiffness.I can't fully move at least two parts of my arm on one side.I can't fully move at least two parts of my arm on one side.
Research Study Groups:
This trial has the following groups:- Group 1: Treatment Arm
- Group 2: Control Arm
Awards:
This trial has 0 awards, including: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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