Last updated on December 2018

Evaluation of the Effectiveness and Tolerance of Tetracosactide Synacthen in the Treatment of Post Dural Puncture Headaches (ESYBRECHE)


Brief description of study

The aim of the study is to assess the efficacy and safety of Synacthne 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 Study Identifier: NCT02813655

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Recruitment Status: Open


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