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AuthorisedPhase II and Phase III (Integrated)Interventional
Effect of intravenous immunoglobulins on painful sensory neuropathy evaluated by aggregated N-of-one trials
At a glance
Status
Authorised
Phase
Phase II and Phase III (Integrated)
Sponsor
Sorlandet Sykehus HF
Enrolment target
30
Start
09 Dec 2022
What is this study about?
Pain intensity the second week (mean of days 8, 10 and 13) after start of IVIG/placebo infusions scored on a numeric rating scale (NRS) ranging from 0 to 10
Who may be eligible?
Age 18 Years to any · Sex: All
Locations (1)
- —Norway
How to find out more
Always speak to your GP or specialist before deciding to take part in a study.
Discussion
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