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Active, Not Recruiting

NCT Number: NCT03306615

Peripheral Modulation of Muscle Stiffness and Spasticity

This is a single-center, double-blind, randomized, placebo-controlled, sequential Phase II trial of human recombinant hyaluronidase injections in individuals with post-stroke upper limb muscle stiffness. The investigators will recruit 56 subjects, who will be randomized to receive either the intervention or normal saline injections (first injection), and then the intervention the participants did not receive first (second injection). All individuals will receive the treatment by the end of the study.

Active, Not Recruiting

This study is active but is not currently recruiting participants.

Key information

About this study

  • To test the effect of hyaluronidase injections on upper limb outcomes. The investigators will test the hypothesis that compared to placebo, human recombinant hyaluronidase injections will increase passive range of motion (ROM) in the most affected joint of the upper limb (primary outcome), isometric muscle strength or force generation capacity using Maximum Voluntary Contraction (MVC) on electromyography (EMG), reduce upper limb motor impairment as measured by the Fugl-Meyer (FM) scale, and improve function as measured by the Wolf Motor Function Test (WMFT).
  • To evaluate the effect of hyaluronidase on neural and non-neural components of muscle stiffness. The investigators will test the hypothesis that compared to placebo, intramuscular (IM) hyaluronidase will modulate the passive and potentially also the active component of the stretch reflex, reduce stiffness and improve arm motor control.
  • To determine the effect of hyaluronidase on intramuscular glycosaminoglycans (GAG) content. The investigators will test the hypothesis that compared to placebo, IM hyaluronidase will reduce the T1rho relaxation times in the biceps and triceps muscles of the affected arm.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Ischemic or hemorrhagic stroke 4-180 months prior
  • Moderately-severe muscle stiffness
  • Lack of full passive and active range of motion in at least 2/4 areas (shoulder, elbow, forearm, wrist) in the hemiparetic upper limb;
  • Willingness to have MRI, complete all clinical assessments, and comply with study protocols;
  • Ability to give informed consent and HIPPA certifications; and

Exclusion criteria

  • treatment of spasticity with Botulinum toxin or intrathecal baclofen within the past six months, phenol injections within the past 12 months, or ongoing adjustment of anti-spastic medications;
  • other neurologic condition that may affect motor response (e.g., Parkinson's disease, amyotrophic lateral sclerosis (ALS), MS);
  • clinically significant cognitive dysfunction with score <19 on Folstein's Mini Mental Status Examination or depression with score >10 on the Patient Health Questionnaire-9 (PHQ-9);
  • pregnancy;
  • known hypersensitivity to hyaluronidase;
  • claustrophobia;
  • standard contraindications for MRI
  • Any condition that will preclude the patient from completing the protocol as determined by the PI

Treatment and study plan

Hyaluronidase

Drug

HYLENEX recombinant, diluted with 0.9% Sodium Chloride Injection

Other names: Hylenex

Placebo

Drug

0.9% Sodium Chloride Injection

Other names: Normal saline

Primary outcomes

  1. Most affected upper limb joint passive range of motion (Cohort 1)

    Time frame: 9 weeks

    passive range of motion in most affected joint across the upper limb

  2. Most affected upper limb joint passive range of motion (Cohort 2)

    Time frame: 15 weeks

    passive range of motion in most affected joint across the upper limb

Secondary outcomes

  1. Total upper limb passive and active range of motion

    Time frame: 15 weeks

    passive and active range of motion in shoulder, elbow and forearm joints

  2. Change in upper limb Fugl-Meyer Assessment Score

    Time frame: 15 weeks

    measures motor impairment in the affected upper limb, Score range is 0-66, and a higher score indicates a better outcome

  3. Change in Wolf-Motor Function Test (WMFT) Score

    Time frame: 15 weeks

    Measures upper extremity function following stroke, Includes 6 items, with a 0-5 score range for each item, and a higher score indicates a better outcome

Sponsors and collaborators

Lead sponsor

Johns Hopkins University

Other

Collaborators

  • Sheikh Khalifa Stroke Institute

Registry information

Important dates

Study start
2021
Primary completion
2026
Study completion
2027
First posted
Oct 11, 2017
Registry last updated
Jun 30, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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