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Lumbar Drainage of Intraventricular Hemorrhage

Lumbar Drainage of Intraventricular Hemorrhage The DRAIN IVH Randomized Controlled Trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06510842
Acronym
DRAIN IVH
Enrollment
354
Registered
2024-07-19
Start date
2025-01-16
Completion date
2029-07-01
Last updated
2026-01-28

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

Conditions

External Ventricular Drainage, Intraventricular Hemorrhage, Lumbar Drainage

Brief summary

Intracerebral hemorrhage (ICH) is a debilitating and fatal disease, especially when the hemorrhage is also entering the cerebral ventricles leading to acute hydrocephalus. In these cases, patients need a drainage through external ventricular drains (EVD). In the longer term, patients often need a permanent ventriculoperitoneal (VP) shunt to avoid hydrocephalus. Here we hypothesize that the early insertion of a lumbar drainage in addition to the EVD could lead to better functional outcome and avoidance of VP shunting by drainage of the blood which promotes inflammatory and adverse effects in the subarachnoid space. For that we propose a multi-center randomized clinical trial to investigate the hypothesis.

Interventions

OTHERExternal drainage of intraventricular hemorrhage

An EVD is required to be eligible for the DRAIN IVH study. Weaning from the EVD is at the discretion of the local investigators. Imaging is at discretion of local investigators. Use, timing and frequency of fibrinolysis via EVD is at local discretion, too.

Sponsors

University Hospital Heidelberg
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

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

Inclusion criteria

* ICH with IVH (with hemorrhage in the 3rd and/or 4rth ventricle) with the need for EVD placement due to acute hydrocephalus * Age ≥ 18 y * Lumbar drain can be inserted within 72 h after symptom onset or patient last seen well

Exclusion criteria

* Premorbid mRS score \> 2 * Pregnancy * Life expectancy \<6 months * Patient/family/caregiver unwilling or unlikely to opt for at least two weeks of aggressive therapy prior to consideration of transition to comfort measures/discontinuation of life support measures. * Treating physicians deeming the prognosis as so grave that an aggressive therapy is not warranted. * Other clear contraindication for treatment with a lumbar drain

Design outcomes

Primary

MeasureTime frameDescription
Rate of mRS180 days (+/- 14 days)The mRS is frequently employed to assess functional outcome of stroke therapy - its ease of use, simplicity of interpretation for clinicians and families, and agreement with other stroke scales are appealing features. The use of fixed dichotomous analysis of ordered categorical outcomes after stroke (mRS 0-3 favorable vs. 4-6 non-favorable outcome) has proved to be valid and reliable for defining outcome in stroke patients in many previous studies.

Secondary

MeasureTime frameDescription
Amount of CSF drained by external ventricular drainup to 14 days (duration of hospital stay)in ml
Amount of CSF drained by lumbar drainup to 14 days (duration of hospital stay)in ml
Need for VP shuntup to 14 days (duration of hospital stay)operative implantation of VP shunt
Clearance of intraventricular blood (via neuroimaging with CT or MRI)up to 14 days (duration of hospital stay)Opening of third ventricle (y/n)
Bacterial Ventriculitis/Meningitis leading to antibiotic treatmentup to 14 days (duration of hospital stay)(y/n)
Mortalityup to 14 days (duration of hospital stay) and 6 monthcerebral cause of death (y/n)

Countries

Germany

Contacts

CONTACTSilvia Schönenberger, MD
silvia.schoenenberger@med.uni-heidelberg.de0049/6221/567504
CONTACTMin Chen, MD
min.chen@med.uni-heidelberg.de0049/6221/567504
PRINCIPAL_INVESTIGATORSilvia Schönenberger, MD

Heidelberg University Hospital, Department of Neurology

Outcome results

None listed

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