Botulinum Toxin Type A for Neuroma Pain
Withdrawn before enrolling · Phase 2 · Has a placebo group
Conditions studied: Neuroma
In brief
The purpose of this study is to determine if botulinum toxin type A (Btx-A) is an effective treatment for painful neuromas. The ideal therapy for painful neuromas would be effective, non-addictive, safe, localized, and cost-effective treatment. At the same time, the therapy would also address the complex peripheral and central mechanisms. Btx-A is a potential treatment that addresses each of these requirements while preserving the existing sensation and function. Study Hypothesis: Btx-A injection relieves neuroma pain better than a placebo
Key facts
- Study ID
- NCT01374191
- Run by
- Southern Illinois University
- People needed
- 0
- Starts
- 2015-01-01
- Expected to finish
- 2017-09-01
- Last updated by the study team
- 2015-08-26
Who can join
Age: 18 and older, up to 75. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Male or female
- aged 18-75 years
- diagnosed with neuroma pain
- able to return/be available for follow-up evaluations
- willingness and ability to give informed consent
You may not qualify if…
- positive for HIV/AIDS or otherwise immunocompromised
- history of neuromuscular disease
- reported allergy to BOTOX®
- history or symptoms of any significant medical problem in the last year (i.e., bradycardia, impaired cardiovascular function, liver disease)
- symptoms of infection or illness with initial enrollment
- pregnant or lactating women
- unable or unwilling to maintain abstinence or use contraception for 28 days following all injections
- cognitively impaired patients unable to give informed consent
Where it is running
- Southern Illinois University School of Medicine — Springfield, Illinois, United States
Full record on ClinicalTrials.gov
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