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HES Patch Versus Blood Patch

Clinical Effect and Cerebral Vasoconstriction Induced After Epidural Blood Patch Versus Epidural Hydroxyethyl Starch Patch in Patients With Headache Due to Intracranial Hypotension

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02570724
Enrollment
20
Registered
2015-10-07
Start date
2013-06-30
Completion date
2018-08-31
Last updated
2019-08-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Intracranial Hypotension

Brief summary

The injection of autologous blood Blood Patch (BP) into the epidural space is the standard treatment for headache associated with intracranial hypotension. It provokes cerebral vasoconstriction. It is cons-indicated in a number of situations (HIV positive, fever, sepsis, leukemia). The purpose of this study is to evaluate another technique using a patch made by injecting an epidural hydroxyethylstarch solution (HES 130, 0.4, 6%) instead of blood patch. This alternative technique is simple to implement and does not have some of the specific blood pressure contra-indications. The study aims at comparing the Blood Patch group versus the HES Patch in terms of clinical efficacy , tolerance, satisfaction of the anesthetist, ease of implementation and effect of the injection of epidural anesthesia on cerebral blood flow within 24 hours.

Interventions

DRUGinjection of HES Voluven®

Injection into the epidural space of 15 to 30 ml Voluven ® at a rate of 1 ml / about 5 seconds.

BIOLOGICALblood patch

Sponsors

University Hospital, Strasbourg, France
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Subjects older than 18 years.· * Subjects with an intracranial hypertension syndrome secondary to an epidural, spinal or lumbar puncture (and therefore presumed iatrogenic) with a sub arachnoid space or subjects with intracranial hypertension syndrome of primitive origin requiring treatment with epidural Patch · * subjects with a temporal window of sufficient quality to carry out the transcranial Doppler · * Subjects haven read the informed consent, signed and dated prior to the start of any proceedings related to the tial· * Subjects affiliated to health insurance· * Subjects having been informed of the results of a prior medical consultation

Exclusion criteria

* Subjects with a cons-indication to an epidural Patch: * blood disorders constitutional or acquired coagulation with platelets * Subjects under treatment with curative doses of antiplatelet drugs or anticoagulants * subjects under shock and / or hypovolemia * subjects under generalized sepsis or at the puncture site * any other cons-indication to performing an epidural

Design outcomes

Primary

MeasureTime frameDescription
Variation of the pulsatility index (PI) of the middle cerebral artery transcranial Doppler36 hoursCompare the effect of epidural injection of autologous blood (Blood Patch) versus injection of a colloid (HES Voluven ®) on cerebral blood flow. this study aims at observing the variation of the pulsatility index (PI) of middle cerebral artery observed by a transcranial Doppler between T0 and 30 minutes after the patch is administered. The BP or HEA treatment will be considered equivalent if the proportion of clinical failures and side effects do not differ by more than 5%.

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026