Lead Sponsor

Centre Hospitalier Universitaire de Nīmes

Age

18 - No limit years

Sex

FEMALE

Healthy Volunteers

No

•The patient was informed about the implementation of the study, its objectives, constraints and patient rights
•The patient has signed the informed consent
•The patient must be affiliated or beneficiary of a health insurance plan
•The patient is available for follow up concerning her hospital stay
•The patient has a post-dural puncture headache after a vaginal delivery. The diagnosis of post-puncture headache is retained on the basis of a frankly postural character for the headache, triggered or exacerbated by orthostatic position and relieved by recumbency.
•The patient has an indication for a blood patch

•The patient is participating in another interventional study, with the exception of the following studies: Papillo PMA (2013-A00538-37); DG-Postpartum (2013-A00277-38); ElastoMAP (2013-A01148-37); ElastoDéclench (2014-A00828-39); LXRs(2009-A00968-49); OASIS II (2013-A00773-42); GrossPath (2014-A01120-47).
•The patient is in an exclusion period determined by a previous study
•The patient is under guardianship, curatorship or under judicial protection
•The patient refuses to sign the consent
•It is not possible correctly inform the patient
•The patient is pregnant
•The patient has a contra-indication (or an incompatible combination therapy) for a necessary treatment in this study
•The patient was delivered by cesarean section

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