An open study to compare the efficacy of immunoglobulin administered subcutaneoulsy (SCIG) with current best practice in patients with Complex Regional Pain Syndrome (CRPS)

Registry ID
EUCTR2009-015242-30
Source registry
EUCTR
Status
Prematurely Ended
Phase
PHASE4
Sponsor
The Walton Centre for Neurology and Neurosurgery NHS Trust
Start date
2009-11-05
Completion date
2011-11-07
Last update
2026-08-16

Conditions

Summary

To ascertain the efficacy of repeated doses over one year of immune modulation treatment with a subcutaneous preparation of immunoglobulins (SCIG) in patients who had pain relief after a single dose intravenous immunoglobulin treatment.

Locations

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