CompletedPhase 3NCT02165111
Efficacy of Botulinum Toxin In Scleroderma-Associated Raynaud's Syndrome
Studying Scleroderma
Last synced from ClinicalTrials.gov
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Report missing dataKey facts
- Sponsor
- Johns Hopkins University
- Principal Investigator
- Scott D Lifchez, MD, MD, MHSJohns Hopkins University
- Intervention
- Onabotulinumtoxin A(drug)
- Enrollment
- 40 target
- Eligibility
- 18 years · All sexes
- Timeline
- 2015 – 2015
Study locations (1)
- Johns Hopkins Bayview Medical Center, Baltimore, Maryland, United States
Collaborators
Allergan
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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