Johns Hopkins School of Medicine
Baltimore, Maryland, 21231, United States
NCT Number: NCT03306615
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.
This study is active but is not currently recruiting participants.
18 year and older
All sexes
Interventional
Phase 2
Baltimore, Maryland, 21231, United States
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
HYLENEX recombinant, diluted with 0.9% Sodium Chloride Injection
Other names: Hylenex
0.9% Sodium Chloride Injection
Other names: Normal saline
Time frame: 9 weeks
passive range of motion in most affected joint across the upper limb
Time frame: 15 weeks
passive range of motion in most affected joint across the upper limb
Time frame: 15 weeks
passive and active range of motion in shoulder, elbow and forearm joints
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
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
Johns Hopkins University
Other
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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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