Overview

The Effect of Abobotulinum Toxin A on the Symptoms of Raynaud's Phenomenon

Status:
Terminated
Trial end date:
2020-01-31
Target enrollment:
0
Participant gender:
All
Summary
This study aims to investigate the effect of abobotulinum toxin A on the symptoms of Raynaud's phenomenon.
Phase:
Phase 4
Accepts Healthy Volunteers?
Accepts Healthy Volunteers
Details
Lead Sponsor:
University of Central Florida
Treatments:
abobotulinumtoxinA
Botulinum Toxins, Type A
onabotulinumtoxinA
Pharmaceutical Solutions
Criteria
Inclusion Criteria:

- Male or female adult between 18 and 80 years of age

- Must have health insurance

- Must have a current diagnosis of Raynaud's phenomenon

Exclusion Criteria:

- Allergy to abobotulinum toxin A or its components

- Diagnosis of myasthenia gravis

- Previously received abobotulinum toxin vaccine

- Previously undergone upper extremity vascular surgery (including surgical
sympathectomy)

- Currently receiving aminoglycoside antibiotics

- Received abobotulinum toxin A treatment in either hand in the past 6 months

- Pregnant women

- Women currently breastfeeding

- Current tobacco smoker (use in the past 12 months)

- Unable to read and speak English

- Adults unable to consent

- Individuals who are not yet adults (infants, children, teenagers)

- Prisoners