Clinical Trials Directory

Trials / Terminated

TerminatedNCT02427009

Maintaining a Prone Position After Use of an Epidural Blood Patch for the Treatment of Post-dural Puncture Headache

Effectiveness of Maintaining a Prone Position After Use of an Epidural Blood Patch for the Treatment of Post-dural Puncture Headache

Status
Terminated
Phase
N/A
Study type
Interventional
Enrollment
3 (actual)
Sponsor
Centre Hospitalier Universitaire de Nīmes · Academic / Other
Sex
Female
Age
18 Years
Healthy volunteers
Not accepted

Summary

The main objective of this study is to assess the rate of recurrence of headache following a first blood patch where patients will be positioned in the prone position for an hour after each blood patch needed during this study.

Detailed description

The secondary objectives of this study are to: A. To evaluate the number of blood patches needed for each patient during her hospital stay B. Assessing the intensity of all headaches every 24H C. Evaluate the complications occurring during the hospital stay.

Conditions

Interventions

TypeNameDescription
OTHERProne position for 1 hour after blood patchAfter performing a blood patch, the patient will be placed in a prone position for 1 hour. This applies to all blood patches required during her hospitalization.
PROCEDUREBlood patchAnd indicated in inclusion criteria, patients in this protocol will have at least 1 blood patch. The amount of blood to be injected into the peridural space is fixed at 20 ml, but can be less in case of pain.

Timeline

Start date
2015-12-01
Primary completion
2016-04-21
Completion
2016-04-23
First posted
2015-04-27
Last updated
2017-02-01

Locations

1 site across 1 country: France

Source: ClinicalTrials.gov record NCT02427009. Inclusion in this directory is not an endorsement.