Raynaud'
Conditions
Interventions
No treatment
Low dose of botulinum toxin injection
Medium dose of botulinum toxin injection
High dose of botulinum toxin injection
Sponsors
Gunma University Hospital
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: All patients fulfilled the criteria of SSc proposed by the American College of Rheumatology and the American College of Rheumatology/European League Against Rheumatism classification criteria.
Exclusion criteria
Exclusion criteria: Patients under the age 18, with the pregnancy or having the past medical histories with BTX were excluded.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The change in severity of RP, including the frequency, pain, color and duration, by the Raynaud score and VAS at 4 weeks after treatment compared with the baseline. | — |
Countries
Japan
Contacts
Public ContactSei-ichiro Motegi
Gunma University Graduate School of Medicine Department of Dermatology
Outcome results
None listed