Treatment of Plantar Fasciitis With Xeomin (Xeomin)
Primary Purpose
Plantar Fascitis
Status
Completed
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
Xeomin
Sponsored by
About this trial
This is an interventional treatment trial for Plantar Fascitis focused on measuring plantar fascia, plantar fascitis, botulinum toxin, Xeomin
Eligibility Criteria
Inclusion Criteria:
- Subjects will be adults above the age of 18 years of any gender or race.
- Subjects' diagnosis will be plantar fasciitis.
- Subjects should have attempted 6 weeks of nonsurgical treatment and failed prior to injection.
Exclusion Criteria:
- Subjects must not have a normal plantar fascia.
- Subjects must not have received previous BoTox injections at their plantar fascia.
- Subjects must have not have received prior surgery on their plantar fascia.
Sites / Locations
- Rothman Institute Orthopaedics
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Placebo Comparator
Arm Label
Xeomin
Placebo
Arm Description
Group A will consist of 25 patients that receive Xeomin. Group B will contain the other 25 patients that receive the placebo saline solution. Post-injection treatment will be kept the same between the two groups. This will only consist of plantar fascial stretching done 3 times daily.
Group B will contain the other 25 patients that receive the placebo saline solution. Post-injection treatment will be kept the same between the two groups. This will only consist of plantar fascial stretching done 3 times daily.
Outcomes
Primary Outcome Measures
Function
Function will be scored primarily according to the Foot and Ankle Ability Measure (FAAM), which is validated and reproducible. Scores are based on standing, walking, and performing activities of daily living (ADLs). The scores are between 0 points for being completely disabled and 100 points for being totally without symptoms. A score of 90 or more indicates an excellent result. The PI will gather scores before and after injection. These FAAM scores will be gathered at the time of outpatient follow-up and used to evaluate the final outcome.
Secondary Outcome Measures
Pain
Patients' pain will be scored with a 10 cm visual analog scale (VAS). If applicable, progression to surgical treatment will also be documented.
Full Information
NCT ID
NCT01678001
First Posted
August 30, 2012
Last Updated
January 13, 2017
Sponsor
Rothman Institute Orthopaedics
Collaborators
Merz North America, Inc.
1. Study Identification
Unique Protocol Identification Number
NCT01678001
Brief Title
Treatment of Plantar Fasciitis With Xeomin
Acronym
Xeomin
Official Title
Treatment of Plantar Fasciitis With Xeomin: A Randomized, Placebo-Controlled, Double-Blinded, Prospective Study
Study Type
Interventional
2. Study Status
Record Verification Date
January 2017
Overall Recruitment Status
Completed
Study Start Date
August 2012 (undefined)
Primary Completion Date
August 2016 (Actual)
Study Completion Date
August 2016 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Rothman Institute Orthopaedics
Collaborators
Merz North America, Inc.
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The plantar fascia is an inelastic, broad band of tissue on the plantar or undersurface of the foot.
Plantar fasciitis is an inflammation of the plantar fascia that causes heel and foot pain.
The current standard orthopaedic management of plantar fasciitis begins with nonsurgical treatment modalities. Surgical treatment of plantar fasciitis is indicated only if nonsurgical means fail.
A newer method of treating plantar fasciitis before resorting to surgery is the use of Botulinum Toxin or Xeomin (incobotulinum toxin A, Merz USA). Treatment of plantar fasciitis with Xeomin is important, as there are limited studies on the subject to date. The purpose of this study is to examine the long-term results of using Xeomin to treat plantar fasciitis in one physician's (J.A.) practice at Rothman Institute Orthopaedics through a placebo-controlled, randomized, double-blinded study.
Detailed Description
The plantar fascia is an inelastic, broad band of muscle on the plantar or undersurface of the foot. It runs from the plantar surface of the calcaneus or heel bone to the plantar surface of all 5 toes. The plantar fascia maintains the arch shape of the plantar foot. It also helps with shock absorption upon weight bearing activities such as walking and running.
Plantar fasciitis is an inflammation of the plantar fascia that causes heel and foot pain. This inflammation is often caused by over activity, improper shoes, flat feet, or excessive weight on the feet.
The current standard orthopaedic management of plantar fasciitis begins with nonsurgical treatment modalities. Such methods include daily stretching of the fascia, foot orthotics or inserts to provide arch support, night splinting, and shock-wave therapy. Surgical treatment of plantar fasciitis is indicated only if nonsurgical means fail. However, surgery does have risks, which include but are not limited to bleeding, infection, and nerve injury.
A newer method of treating plantar fasciitis before resorting to surgery is the use of Botulinum Toxin or Xeomin (incobotulinum toxin A, Merz USA). Xeomin can only be delivered via direct injection into the targeted muscle. It takes effect in 2 to 3 days and generally lasts up to 3 to 6 months. Some doctors give Xeomin injections every 3 months or longer for treating spastic muscles. However, others provide single injections to help achieve a specific goal.
Treatment of plantar fasciitis with Xeomin is important, as there are limited studies on the subject to date. Much of the existing research involves BoTox A and non-controlled studies with less than 1 year of patient follow-up. To date, there is only 1 placebo-controlled, randomized, double-blinded study regarding BoTox A to treat plantar fasciitis. However, this study limits its follow-up to 8 weeks. The purpose of this study is to examine the long-term results of using Xeomin to treat plantar fasciitis in one physician's (J.A.) practice at Rothman Institute Orthopaedics through a placebo-controlled, randomized, double-blinded study.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Plantar Fascitis
Keywords
plantar fascia, plantar fascitis, botulinum toxin, Xeomin
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
50 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Xeomin
Arm Type
Active Comparator
Arm Description
Group A will consist of 25 patients that receive Xeomin. Group B will contain the other 25 patients that receive the placebo saline solution. Post-injection treatment will be kept the same between the two groups. This will only consist of plantar fascial stretching done 3 times daily.
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Group B will contain the other 25 patients that receive the placebo saline solution. Post-injection treatment will be kept the same between the two groups. This will only consist of plantar fascial stretching done 3 times daily.
Intervention Type
Drug
Intervention Name(s)
Xeomin
Intervention Description
Group A will consist of 25 patients that receive Xeomin. Group B will contain the other 25 patients that receive the placebo saline solution. Post-injection treatment will be kept the same between the two groups. This will only consist of plantar fascial stretching done 3 times daily.
Primary Outcome Measure Information:
Title
Function
Description
Function will be scored primarily according to the Foot and Ankle Ability Measure (FAAM), which is validated and reproducible. Scores are based on standing, walking, and performing activities of daily living (ADLs). The scores are between 0 points for being completely disabled and 100 points for being totally without symptoms. A score of 90 or more indicates an excellent result. The PI will gather scores before and after injection. These FAAM scores will be gathered at the time of outpatient follow-up and used to evaluate the final outcome.
Time Frame
1 year
Secondary Outcome Measure Information:
Title
Pain
Description
Patients' pain will be scored with a 10 cm visual analog scale (VAS). If applicable, progression to surgical treatment will also be documented.
Time Frame
1 year
Other Pre-specified Outcome Measures:
Title
Satisfaction
Description
Patients will be asked about their satisfaction by using a CGI satisfaction scale.
Time Frame
1 year
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Subjects will be adults above the age of 18 years of any gender or race.
Subjects' diagnosis will be plantar fasciitis.
Subjects should have attempted 6 weeks of nonsurgical treatment and failed prior to injection.
Exclusion Criteria:
Subjects must not have a normal plantar fascia.
Subjects must not have received previous BoTox injections at their plantar fascia.
Subjects must have not have received prior surgery on their plantar fascia.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jamal Ahmad, M.D.
Organizational Affiliation
Rothman Institute Orthopaedics
Official's Role
Principal Investigator
Facility Information:
Facility Name
Rothman Institute Orthopaedics
City
Philadelphia
State/Province
Pennsylvania
ZIP/Postal Code
19107
Country
United States
12. IPD Sharing Statement
Learn more about this trial
Treatment of Plantar Fasciitis With Xeomin
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