Dose-response Relationship of Botullinum Toxin (DWP 450) for Finger Flexor Spasticity
Primary Purpose
Spasticity as Sequela of Stroke
Status
Unknown status
Phase
Phase 4
Locations
Korea, Republic of
Study Type
Interventional
Intervention
Normal Saline 0.9% 1.2 ml
Clostridium Botulinum Toxin Type A (Nabota, DWP 450) 15 U
Clostridium Botulinum Toxin Type A (Nabota, DWP 450) 30 U
Clostridium Botulinum Toxin Type A (Nabota, DWP 450) 50 U
Clostridium Botulinum Toxin Type A (Nabota, DWP 450) 70 U
Sponsored by
About this trial
This is an interventional treatment trial for Spasticity as Sequela of Stroke
Eligibility Criteria
Inclusion Criteria:
- over 6 weeks after stroke onset
- MAS (modified Ashworth scale) greater than 2 in finger flexor
Exclusion Criteria:
- neuromuscular junction disease or motor neuron disease
- phenol or alcohol block for the target limbs within 6 months before screening
- botulinum toxin injection within 3 months before screening
- history or plan for tendon lengthening surgery
- significant contracture ormuscle atrophy at the target joint or muscle
- concurrent treatment with intrathecal baclofen
- hypersensitivity or allergy to study drug or its components
- pregnancy or planned pregnancy, breastfeeding
- abnormal lab findings for alanine aminotransferase, aspartate aminotransferase, blood urea nitrogen, and serum creatinine.
Sites / Locations
- Seoul Metropolitan Government-Seoul National University Boramae Medical CenterRecruiting
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm 4
Arm 5
Arm Type
Placebo Comparator
Experimental
Experimental
Experimental
Experimental
Arm Label
Placebo
Treatment dose 15
Treatment dose 30
Treatment dose 50
Treatment dose 70
Arm Description
Normal Saline 0.9% 1.2 ml will be injected to finger flexor muscles
Clostridium Botulinum Toxin Type A (Nabota, DWP 450) 15 U will be injected to finger flexor muscles
Clostridium Botulinum Toxin Type A (Nabota, DWP 450) 30 U will be injected to finger flexor muscles
Clostridium Botulinum Toxin Type A (Nabota, DWP 450) 50 U will be injected to finger flexor muscles
Clostridium Botulinum Toxin Type A (Nabota, DWP 450) 70 U will be injected to finger flexor muscles
Outcomes
Primary Outcome Measures
MAS (Modified Ashworth Scale)
Spasticity measurement measures resistance during passive soft-tissue stretching(taken from Bohannon and Smith, 1987):
0: No increase in muscle tone
Slight increase in muscle tone, manifested by a catch and release or by minimal resistance at the end of the range of motion when the affected part(s) is moved in flexion or extension 1+: Slight increase in muscle tone, manifested by a catch, followed by minimal resistance throughout the remainder (less than half) of the ROM
More marked increase in muscle tone through most of the ROM, but affected part(s) easily moved
Considerable increase in muscle tone, passive movement difficult
Affected part(s) rigid in flexion or extension
MAS (Modified Ashworth Scale)
Spasticity measurement measures resistance during passive soft-tissue stretching(taken from Bohannon and Smith, 1987):
0: No increase in muscle tone
Slight increase in muscle tone, manifested by a catch and release or by minimal resistance at the end of the range of motion when the affected part(s) is moved in flexion or extension 1+: Slight increase in muscle tone, manifested by a catch, followed by minimal resistance throughout the remainder (less than half) of the ROM
More marked increase in muscle tone through most of the ROM, but affected part(s) easily moved
Considerable increase in muscle tone, passive movement difficult
Affected part(s) rigid in flexion or extension
MAS (Modified Ashworth Scale)
Spasticity measurement measures resistance during passive soft-tissue stretching(taken from Bohannon and Smith, 1987):
0: No increase in muscle tone
Slight increase in muscle tone, manifested by a catch and release or by minimal resistance at the end of the range of motion when the affected part(s) is moved in flexion or extension 1+: Slight increase in muscle tone, manifested by a catch, followed by minimal resistance throughout the remainder (less than half) of the ROM
More marked increase in muscle tone through most of the ROM, but affected part(s) easily moved
Considerable increase in muscle tone, passive movement difficult
Affected part(s) rigid in flexion or extension
MAS (Modified Ashworth Scale)
Spasticity measurement measures resistance during passive soft-tissue stretching(taken from Bohannon and Smith, 1987):
0: No increase in muscle tone
Slight increase in muscle tone, manifested by a catch and release or by minimal resistance at the end of the range of motion when the affected part(s) is moved in flexion or extension 1+: Slight increase in muscle tone, manifested by a catch, followed by minimal resistance throughout the remainder (less than half) of the ROM
More marked increase in muscle tone through most of the ROM, but affected part(s) easily moved
Considerable increase in muscle tone, passive movement difficult
Affected part(s) rigid in flexion or extension
MAS (Modified Ashworth Scale)
Spasticity measurement measures resistance during passive soft-tissue stretching(taken from Bohannon and Smith, 1987):
0: No increase in muscle tone
Slight increase in muscle tone, manifested by a catch and release or by minimal resistance at the end of the range of motion when the affected part(s) is moved in flexion or extension 1+: Slight increase in muscle tone, manifested by a catch, followed by minimal resistance throughout the remainder (less than half) of the ROM
More marked increase in muscle tone through most of the ROM, but affected part(s) easily moved
Considerable increase in muscle tone, passive movement difficult
Affected part(s) rigid in flexion or extension
Secondary Outcome Measures
Ultrasonography
measurement of changes of cross sectional area
Ultrasonography
measurement of changes of cross sectional area
Ultrasonography
measurement of changes of cross sectional area
Ultrasonography
measurement of changes of cross sectional area
Ultrasonography
measurement of changes of cross sectional area
Fugl Myer Upper Extremity Assessment
measurement of upper extremity function
Fugl Myer Upper Extremity Assessment
measurement of upper extremity function
Fugl Myer Upper Extremity Assessment
measurement of upper extremity function
Fugl Myer Upper Extremity Assessment
measurement of upper extremity function
Fugl Myer Upper Extremity Assessment
measurement of upper extremity function
Wolf Motor Assessment
measurement of upper extremity function
Wolf Motor Assessment
measurement of upper extremity function
Wolf Motor Assessment
measurement of upper extremity function
Wolf Motor Assessment
measurement of upper extremity function
Wolf Motor Assessment
measurement of upper extremity function
Full Information
NCT ID
NCT03517319
First Posted
April 17, 2018
Last Updated
May 3, 2018
Sponsor
Seoul National University Hospital
Collaborators
Daewoong Pharmaceutical Co. LTD.
1. Study Identification
Unique Protocol Identification Number
NCT03517319
Brief Title
Dose-response Relationship of Botullinum Toxin (DWP 450) for Finger Flexor Spasticity
Official Title
Dose-response Relationship of Botullinum Toxin (DWP 450) for Finger Flexor Spasticity
Study Type
Interventional
2. Study Status
Record Verification Date
May 2018
Overall Recruitment Status
Unknown status
Study Start Date
September 1, 2016 (Actual)
Primary Completion Date
May 2018 (Anticipated)
Study Completion Date
June 2018 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Seoul National University Hospital
Collaborators
Daewoong Pharmaceutical Co. LTD.
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Study Design: Randomized Single Blind Study Objective: To determine the dose relationship of DWP 450 for finger flexor spasticity Subjects: 78 patients with upper extremity spasticity after CVA Inclusion criteria: Patient who have spasticity (MAS greater than 2 in finger flexors) Methods: Patients will be randomly assigned to one of 5 groups. Gp 1: placebo, Gp 2: 15U, Gp 3: 30 U, Gp 4: 50 U, Gp 5: 75 U
Detailed Description
Seventy-eight patients with upper extremity spasticity after cerebrovascular accident will be recruited and randomly assigned to one of 5 groups. The groups are as followings.
Gp 1: placebo group (Normal saline 1.2 ml) Gp 2: Clostridium Botulinum Toxin Type A (Nabota, DWP 450) 15 U Gp 3: Clostridium Botulinum Toxin Type A (Nabota, DWP 450) 30 U Gp 4: Clostridium Botulinum Toxin Type A (Nabota, DWP 450) 50 U Gp 5: Clostridium Botulinum Toxin Type A (Nabota, DWP 450) 70 U
According to the group, the injection will be performed to the finger flexor musles (flexor digitorum superficialis and profundus). Outcome measurement will be MAS (Modified ashworth scale), FMA, Wolf Motor Assessment, Cross sectional area measured by Ultrasonography.
Patient evaluation will be conducted 2 weeks, 1 months, 2 months, and 3 months after the injection.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Spasticity as Sequela of Stroke
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Single Group Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
78 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Normal Saline 0.9% 1.2 ml will be injected to finger flexor muscles
Arm Title
Treatment dose 15
Arm Type
Experimental
Arm Description
Clostridium Botulinum Toxin Type A (Nabota, DWP 450) 15 U will be injected to finger flexor muscles
Arm Title
Treatment dose 30
Arm Type
Experimental
Arm Description
Clostridium Botulinum Toxin Type A (Nabota, DWP 450) 30 U will be injected to finger flexor muscles
Arm Title
Treatment dose 50
Arm Type
Experimental
Arm Description
Clostridium Botulinum Toxin Type A (Nabota, DWP 450) 50 U will be injected to finger flexor muscles
Arm Title
Treatment dose 70
Arm Type
Experimental
Arm Description
Clostridium Botulinum Toxin Type A (Nabota, DWP 450) 70 U will be injected to finger flexor muscles
Intervention Type
Drug
Intervention Name(s)
Normal Saline 0.9% 1.2 ml
Intervention Type
Drug
Intervention Name(s)
Clostridium Botulinum Toxin Type A (Nabota, DWP 450) 15 U
Other Intervention Name(s)
Nabota (DWP 450)
Intervention Type
Drug
Intervention Name(s)
Clostridium Botulinum Toxin Type A (Nabota, DWP 450) 30 U
Other Intervention Name(s)
Nabota (DWP 450)
Intervention Type
Drug
Intervention Name(s)
Clostridium Botulinum Toxin Type A (Nabota, DWP 450) 50 U
Other Intervention Name(s)
Nabota (DWP 450)
Intervention Type
Drug
Intervention Name(s)
Clostridium Botulinum Toxin Type A (Nabota, DWP 450) 70 U
Other Intervention Name(s)
Nabota (DWP 450)
Primary Outcome Measure Information:
Title
MAS (Modified Ashworth Scale)
Description
Spasticity measurement measures resistance during passive soft-tissue stretching(taken from Bohannon and Smith, 1987):
0: No increase in muscle tone
Slight increase in muscle tone, manifested by a catch and release or by minimal resistance at the end of the range of motion when the affected part(s) is moved in flexion or extension 1+: Slight increase in muscle tone, manifested by a catch, followed by minimal resistance throughout the remainder (less than half) of the ROM
More marked increase in muscle tone through most of the ROM, but affected part(s) easily moved
Considerable increase in muscle tone, passive movement difficult
Affected part(s) rigid in flexion or extension
Time Frame
baseline
Title
MAS (Modified Ashworth Scale)
Description
Spasticity measurement measures resistance during passive soft-tissue stretching(taken from Bohannon and Smith, 1987):
0: No increase in muscle tone
Slight increase in muscle tone, manifested by a catch and release or by minimal resistance at the end of the range of motion when the affected part(s) is moved in flexion or extension 1+: Slight increase in muscle tone, manifested by a catch, followed by minimal resistance throughout the remainder (less than half) of the ROM
More marked increase in muscle tone through most of the ROM, but affected part(s) easily moved
Considerable increase in muscle tone, passive movement difficult
Affected part(s) rigid in flexion or extension
Time Frame
2wks after injection
Title
MAS (Modified Ashworth Scale)
Description
Spasticity measurement measures resistance during passive soft-tissue stretching(taken from Bohannon and Smith, 1987):
0: No increase in muscle tone
Slight increase in muscle tone, manifested by a catch and release or by minimal resistance at the end of the range of motion when the affected part(s) is moved in flexion or extension 1+: Slight increase in muscle tone, manifested by a catch, followed by minimal resistance throughout the remainder (less than half) of the ROM
More marked increase in muscle tone through most of the ROM, but affected part(s) easily moved
Considerable increase in muscle tone, passive movement difficult
Affected part(s) rigid in flexion or extension
Time Frame
4wks after injection
Title
MAS (Modified Ashworth Scale)
Description
Spasticity measurement measures resistance during passive soft-tissue stretching(taken from Bohannon and Smith, 1987):
0: No increase in muscle tone
Slight increase in muscle tone, manifested by a catch and release or by minimal resistance at the end of the range of motion when the affected part(s) is moved in flexion or extension 1+: Slight increase in muscle tone, manifested by a catch, followed by minimal resistance throughout the remainder (less than half) of the ROM
More marked increase in muscle tone through most of the ROM, but affected part(s) easily moved
Considerable increase in muscle tone, passive movement difficult
Affected part(s) rigid in flexion or extension
Time Frame
8wks after injection
Title
MAS (Modified Ashworth Scale)
Description
Spasticity measurement measures resistance during passive soft-tissue stretching(taken from Bohannon and Smith, 1987):
0: No increase in muscle tone
Slight increase in muscle tone, manifested by a catch and release or by minimal resistance at the end of the range of motion when the affected part(s) is moved in flexion or extension 1+: Slight increase in muscle tone, manifested by a catch, followed by minimal resistance throughout the remainder (less than half) of the ROM
More marked increase in muscle tone through most of the ROM, but affected part(s) easily moved
Considerable increase in muscle tone, passive movement difficult
Affected part(s) rigid in flexion or extension
Time Frame
12wks after injection
Secondary Outcome Measure Information:
Title
Ultrasonography
Description
measurement of changes of cross sectional area
Time Frame
baseline
Title
Ultrasonography
Description
measurement of changes of cross sectional area
Time Frame
2wks after injection
Title
Ultrasonography
Description
measurement of changes of cross sectional area
Time Frame
4wks after injection
Title
Ultrasonography
Description
measurement of changes of cross sectional area
Time Frame
8wks after injection
Title
Ultrasonography
Description
measurement of changes of cross sectional area
Time Frame
12wks after injection
Title
Fugl Myer Upper Extremity Assessment
Description
measurement of upper extremity function
Time Frame
baseline
Title
Fugl Myer Upper Extremity Assessment
Description
measurement of upper extremity function
Time Frame
2 wks after injection
Title
Fugl Myer Upper Extremity Assessment
Description
measurement of upper extremity function
Time Frame
4 wks after injection
Title
Fugl Myer Upper Extremity Assessment
Description
measurement of upper extremity function
Time Frame
8 wks after injection
Title
Fugl Myer Upper Extremity Assessment
Description
measurement of upper extremity function
Time Frame
12 wks after injection
Title
Wolf Motor Assessment
Description
measurement of upper extremity function
Time Frame
baseline
Title
Wolf Motor Assessment
Description
measurement of upper extremity function
Time Frame
2 wks after injection
Title
Wolf Motor Assessment
Description
measurement of upper extremity function
Time Frame
4 wks after injection
Title
Wolf Motor Assessment
Description
measurement of upper extremity function
Time Frame
8 wks after injection
Title
Wolf Motor Assessment
Description
measurement of upper extremity function
Time Frame
12 wks after injection
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
over 6 weeks after stroke onset
MAS (modified Ashworth scale) greater than 2 in finger flexor
Exclusion Criteria:
neuromuscular junction disease or motor neuron disease
phenol or alcohol block for the target limbs within 6 months before screening
botulinum toxin injection within 3 months before screening
history or plan for tendon lengthening surgery
significant contracture ormuscle atrophy at the target joint or muscle
concurrent treatment with intrathecal baclofen
hypersensitivity or allergy to study drug or its components
pregnancy or planned pregnancy, breastfeeding
abnormal lab findings for alanine aminotransferase, aspartate aminotransferase, blood urea nitrogen, and serum creatinine.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Shi-Uk Lee, MD, PhD
Email
shiuk.lee@gmail.com
First Name & Middle Initial & Last Name or Official Title & Degree
Min Hyung Lee
Email
0206330@gmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Shi-Uk Lee
Organizational Affiliation
Seoul National University
Official's Role
Study Chair
Facility Information:
Facility Name
Seoul Metropolitan Government-Seoul National University Boramae Medical Center
City
Seoul
State/Province
Dong Jak Ku
ZIP/Postal Code
156-707
Country
Korea, Republic of
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Shi-Uk Lee, MD, PhD
Email
shiuk.lee@gmail.com
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
Dose-response Relationship of Botullinum Toxin (DWP 450) for Finger Flexor Spasticity
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