Botulinum Toxin A Versus Steroids for the Treatment of Chronic Plantar Fasciitis
Primary Purpose
Plantar Fasciitis
Status
Recruiting
Phase
Not Applicable
Locations
Switzerland
Study Type
Interventional
Intervention
Botulinum toxin A
cortisone
Saline
Sponsored by
About this trial
This is an interventional treatment trial for Plantar Fasciitis focused on measuring plantar fasciitis, Botulinum toxin A, Cortisone, RCT
Eligibility Criteria
Inclusion Criteria:
- Clinical symptoms of a plantar fasciitis
- Plantar fasciitis in MRI
- Exclusion of differential diagnoses
- Symptoms more than 3 months
- Absolution of 3 months unsuccessful treatment
- Written informed consent
Exclusion Criteria
- Active differential diagnoses
- Contraindications: pregnancy and breastfeeding, infection at injection sites, allergy against BTX-A
- Previous injections or surgery for plantar fasciitis
- Neurological diseases affecting the peripheral nervous system
Sites / Locations
- Dep, of Orthopaedic Surgery, Inselspital, University of BerneRecruiting
- Department of Orthopaedic Surgery, Kantonsspital LucerneRecruiting
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
Active Comparator
Active Comparator
Placebo Comparator
Arm Label
BTX-A
Cortisone
Saline
Arm Description
Botulinum A toxin is injected each 100 U in both gastrocnemius muscle-bellies and 50 U in the soleus muscle, i.e. a total of 250 U.
Depot Medrol is injected at the plantar fascia insertion site at the calcaneus
Placebo saline is injected in both gastrocnemius muscle-bellies and in the soleus muscle
Outcomes
Primary Outcome Measures
Change from baseline in foot pain
Measured by VAS FA subjective foot score
Secondary Outcome Measures
Change from baseline in patient health
Measured by SF 36
Change from baseline in pain, disability and activity restriction in foot
Measured by foot functional index FFI
General pain
Measured by VAS pain scale
Reduction of inflammation
Measured by MRI
Number of patients with complications
Change from baseline in ankle range of motion
Measured by goniometer
Full Information
NCT ID
NCT02196155
First Posted
July 17, 2014
Last Updated
February 21, 2023
Sponsor
Insel Gruppe AG, University Hospital Bern
Collaborators
Luzerner Kantonsspital
1. Study Identification
Unique Protocol Identification Number
NCT02196155
Brief Title
Botulinum Toxin A Versus Steroids for the Treatment of Chronic Plantar Fasciitis
Official Title
Botulinum Toxin A Versus Steroids for the Treatment of Chronic Plantar Fasciitis: a Randomized Controlled Study
Study Type
Interventional
2. Study Status
Record Verification Date
February 2023
Overall Recruitment Status
Recruiting
Study Start Date
July 2016 (Actual)
Primary Completion Date
December 2024 (Anticipated)
Study Completion Date
December 2024 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Insel Gruppe AG, University Hospital Bern
Collaborators
Luzerner Kantonsspital
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Plantar fasciitis is the classic and most common type of heel pain. Considering the costs for health care and the temporary disability not only for work, plantar fasciitis results in a substantial (and at least partially unnecessary) burden for the Swiss health care system and national economics.
Nonoperative treatment is the mainstay of treating plantar fasciitis. However, so far no treatment has proven to be superior to others, and there is national and international lack of consensus of how to treat plantar fasciitis best.
The investigators believe that the BTX-A injection in the gastrocnemius and the soleus muscles is currently the most promising non-operative approach, because it is considered to treat the disease at its origin (temporary weakening of the tight triceps surae muscle) as opposed to simply alleviate the symptoms (e.g. plantar cortisone and other injections, ESWT).
However, to date there is no evidence in the literature that compares the new, promising technique of BTX-A injection into the gastroc-soleus complex to a sham (saline) injection and to the gold standard steroid injection at the plantar fascia insertion site. With the intended study, this gap is going to be closed.
Detailed Description
Background
Plantar fasciitis is the classic and most common type of heel pain. Extrapolating the rate of 2 million or 0.6% of the US American population being treated for plantar fasciitis every year to Switzerland, the corresponding number of patients would amount to 50'000 patients being treated for plantar fasciitis. Considering the costs for health care and the temporary disability not only for work, plantar fasciitis results in a substantial (and at least partially unnecessary) burden for the Swiss health care system and national economics.
Nonoperative treatment is the mainstay of treating plantar fasciitis. In the literature, numerous operative and nonoperative treatment approaches for plantar fasciitis have been suggested. However, so far no treatment has proven to be superior to others, and there is national and international lack of consensus of how to treat plantar fasciitis best. Numerous prescriptions for unnecessary orthoses, expensive and painful shock waves, and complications following steroid injection could be obviated, when the safe BTX-A injection demonstrates good results.
The investigators believe that the BTX-A injection in the gastrocnemius and the soleus muscles is currently the most promising non-operative approach, because it is considered to treat the disease at its origin (temporary weakening of the tight triceps surae muscle) as opposed to simply alleviate the symptoms (e.g. plantar cortisone and other injections, ESWT).
The high number of level I and II studies suggests that there is need for clarification and evaluation of the efficacy of several non-operative and operative treatment approaches for the chronic plantar fasciitis. However, to date there is no evidence in the literature that compares the new, promising technique of BTX-A injection into the gastroc-soleus complex to a sham (saline) injection and to the gold standard steroid injection at the plantar fascia insertion site. With the intended study, this gap is going to be closed. Objective evaluation of the BTX-A efficacy includes the randomized allocation of patients to the BTX-A, the steroid, or the saline group, the blinded comparison to the sham (saline) injection, and finally the MRI assessment at the beginning and at the end of the followup. With the evidence resulting from this study, patients can be superiorly counseled in the future with regard to efficacy of nonoperative treatment of plantar fasciitis.
Objective
Plantar fasciitis is the classic and most common type of heel pain. Considering the costs for health care and the temporary disability not only for work, plantar fasciitis results in a substantial (and at least partially unnecessary) burden for the Swiss health care system and national economics. However, so far no treatment has proven to be superior to others, and there is national and international lack of consensus of how to treat plantar fasciitis best.
Methods
Patients are randomly allocated to three groups (1 - 3).
- Patient group 1 - combination of physiotherapy, stretching exercises according to DiGiovanni et al and BTX-A injection into the gastroc-soleus complex: One hundred units (U) of toxin are applied to each muscle belly, and 1 application of 50 U is administered to the soleus, making a total of 250 U.
Patient group 2 - physiotherapy, stretching exercises according to DiGiovanni combined with cortisone injection into the plantar fascia
Patient group 3 - physiotherapy, stretching exercises according to DiGiovanni and saline injection into the gastroc-soleus complex (sham control group)
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Plantar Fasciitis
Keywords
plantar fasciitis, Botulinum toxin A, Cortisone, RCT
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantOutcomes Assessor
Allocation
Randomized
Enrollment
54 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
BTX-A
Arm Type
Active Comparator
Arm Description
Botulinum A toxin is injected each 100 U in both gastrocnemius muscle-bellies and 50 U in the soleus muscle, i.e. a total of 250 U.
Arm Title
Cortisone
Arm Type
Active Comparator
Arm Description
Depot Medrol is injected at the plantar fascia insertion site at the calcaneus
Arm Title
Saline
Arm Type
Placebo Comparator
Arm Description
Placebo saline is injected in both gastrocnemius muscle-bellies and in the soleus muscle
Intervention Type
Drug
Intervention Name(s)
Botulinum toxin A
Intervention Description
Researchers discovered in the 1950s that injecting overactive muscles with minute quantities of botulinum toxin type-A would result in decreased muscle activity. Botulinum toxin type-A has this effect because it prevents the vesicle where the acetylcholine is stored from binding to the membrane where the neurotransmitter can be released. Botulinum toxin type-A thus blocks the release of acetylcholine by the neuron. This will effectively weaken the muscle for a period of three to four months.
In addition to its cosmetic applications, Botox is currently used in the treatment of spasms and dystonias, by weakening involved muscles, for the 60-70 day effective period of the drug. The main conditions treated with botulinum toxin are: Cervical dystonia (spasmodic torticollis) (a neuromuscular disorder involving the head and neck), Blepharospasm (excessive blinking) etc..
Intervention Type
Drug
Intervention Name(s)
cortisone
Intervention Type
Drug
Intervention Name(s)
Saline
Primary Outcome Measure Information:
Title
Change from baseline in foot pain
Description
Measured by VAS FA subjective foot score
Time Frame
at 6 weeks, 3, 6 and 12 (24) months
Secondary Outcome Measure Information:
Title
Change from baseline in patient health
Description
Measured by SF 36
Time Frame
at 6 weeks, 3, 6 and 12 (24) months
Title
Change from baseline in pain, disability and activity restriction in foot
Description
Measured by foot functional index FFI
Time Frame
at 6 weeks, 3, 6 and 12 (24) months
Title
General pain
Description
Measured by VAS pain scale
Time Frame
at 6 weeks, 3, 6 and 12 (24) months
Title
Reduction of inflammation
Description
Measured by MRI
Time Frame
pre-intervention and at 12 months
Title
Number of patients with complications
Time Frame
at 6 weeks, 3, 6 and 12 (24) months
Title
Change from baseline in ankle range of motion
Description
Measured by goniometer
Time Frame
at 6 weeks, 3, 6 and 12 (24) months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Clinical symptoms of a plantar fasciitis
Plantar fasciitis in MRI
Exclusion of differential diagnoses
Symptoms more than 3 months
Absolution of 3 months unsuccessful treatment
Written informed consent
Exclusion Criteria
Active differential diagnoses
Contraindications: pregnancy and breastfeeding, infection at injection sites, allergy against BTX-A
Previous injections or surgery for plantar fasciitis
Neurological diseases affecting the peripheral nervous system
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Fabian Krause, PD Dr.
Phone
0041316322220
Email
fabian.krause@insel.ch
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Fabian Krause, PD Dr.
Organizational Affiliation
Dep. of Orthopaedic Surgery, Inselspital, University of Berne, Freiburgstrasse, 3010 Berne, Switzerland
Official's Role
Principal Investigator
Facility Information:
Facility Name
Dep, of Orthopaedic Surgery, Inselspital, University of Berne
City
Berne
ZIP/Postal Code
3010
Country
Switzerland
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Fabian Krause, PD Dr.
Phone
0041316322220
Email
fabian.krause@insel.ch
First Name & Middle Initial & Last Name & Degree
Fabian Krause, PD Dr.
First Name & Middle Initial & Last Name & Degree
Maziar Shafighi, PD Dr.
Facility Name
Department of Orthopaedic Surgery, Kantonsspital Lucerne
City
Lucerne
ZIP/Postal Code
6000
Country
Switzerland
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Lukas Iselin, Dr.
Phone
004141 205 4807
Email
lukas.iselin@luks.ch
First Name & Middle Initial & Last Name & Degree
Lukas Iselin, Dr.
12. IPD Sharing Statement
Citations:
PubMed Identifier
10534247
Citation
Brin MF, Lew MF, Adler CH, Comella CL, Factor SA, Jankovic J, O'Brien C, Murray JJ, Wallace JD, Willmer-Hulme A, Koller M. Safety and efficacy of NeuroBloc (botulinum toxin type B) in type A-resistant cervical dystonia. Neurology. 1999 Oct 22;53(7):1431-8. doi: 10.1212/wnl.53.7.1431.
Results Reference
result
PubMed Identifier
15811212
Citation
Bihari K. Safety, effectiveness, and duration of effect of BOTOX after switching from Dysport for blepharospasm, cervical dystonia, and hemifacial spasm dystonia, and hemifacial spasm. Curr Med Res Opin. 2005 Mar;21(3):433-8. doi: 10.1185/030079905X36396.
Results Reference
result
PubMed Identifier
23386757
Citation
Elizondo-Rodriguez J, Araujo-Lopez Y, Moreno-Gonzalez JA, Cardenas-Estrada E, Mendoza-Lemus O, Acosta-Olivo C. A comparison of botulinum toxin a and intralesional steroids for the treatment of plantar fasciitis: a randomized, double-blinded study. Foot Ankle Int. 2013 Jan;34(1):8-14. doi: 10.1177/1071100712460215.
Results Reference
result
Learn more about this trial
Botulinum Toxin A Versus Steroids for the Treatment of Chronic Plantar Fasciitis
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