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Clinical Trial Summary

The aim of the study is to assess the efficacy and safety of Synacthène® versus placebo in the treatment of post-dural puncture syndrome in patients receiving epidural analgesia, spinal analgesia, or combined spinal-epidural analgesia for labour.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02813655
Study type Interventional
Source Hospices Civils de Lyon
Contact
Status Terminated
Phase Phase 2
Start date October 2016
Completion date November 21, 2022

See also
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