The purpose of this study is to determine whether botulinum toxin A is effective in the treatment of neuropathic pain in patients with diabetic peripheral polyneuropathy.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Enrollment
9
Placebo
St. Paul's Hospital, The Catholic University of Korea
Seoul, South Korea
Pain intensity using numeric rating scale
Time frame: 4 weeks after intervention
Pain intensity using numeric rating scale
Time frame: 1, 8, 12, 24 weeks after intervention
Quality of life using WHOQOL
Time frame: 4,8,12 weeks after intervention
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.