CompletedNot applicableNCT00637533
A Pilot Clinical Trial of Sympathetic Blockade With Botulinum Toxin Type A to Treat Complex Regional Pain Syndrome (CRPS): a Randomized, Double-Blind, Controlled, Crossover Trial.
Studying Complex regional pain syndrome type 1
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Stanford University
- Principal Investigator
- Ian R CarrollStanford University
- Intervention
- Lumbar sympathetic block with Botulinum Toxin type A(procedure)
- Enrollment
- 10 enrolled
- Eligibility
- 21-80 years · All sexes
- Timeline
- 2004 – 2007
Study locations (1)
- Stanford University School of Medicine, Stanford, California, United States
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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