Cerebrospinal Fluid (CSF) Drainage Study

Sponsor
Mayo Clinic (Other)
Overall Status
Completed
CT.gov ID
NCT01420978
Collaborator
(none)
20
2
2
18.1
10
0.6

Study Details

Study Description

Brief Summary

When patients suffer a subarachnoid hemorrhage (bleeding around the brain), they often develop hydrocephalus. This is an enlargement of the fluid-filled spaces (ventricles) in the brain. Standard-of-care treatment includes placing an external ventricular drain (EVD) to drain off fluid. Eventually the EVD is weaned with the goal of removing it. Occasionally a patient does not tolerate this and a permanent surgery needs to be done to internalize a shunt.

Though this is done commonly and routinely throughout the world, there are no good studies to address how to optimally set the EVD level and how fast to wean it. Most set the EVD to a level of around 15 mmHg. The investigators hypothesize that setting the EVD lower (which will allow higher volume Cerebrospinal Fluid (CSF) drainage through the EVD) will improve perfusion at the level of the microcirculation in the brain, and result in improved neurologic outcomes.

Condition or Disease Intervention/Treatment Phase
  • Procedure: CSF Diversion
N/A

Study Design

Study Type:
Interventional
Actual Enrollment :
20 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
High Volume Cerebrospinal Fluid Diversion in the Management of Aneurysmal Subarachnoid Hemorrhage: A Pilot Study
Study Start Date :
Aug 1, 2011
Actual Primary Completion Date :
Feb 1, 2013
Actual Study Completion Date :
Feb 1, 2013

Arms and Interventions

Arm Intervention/Treatment
Experimental: High volume CSF diversion

The EVD will be set to an initial level of 5 mmHg. The drain will remain in place at a level of ≤ 5 mmHg until at least day 10 after SAH before a weaning trial is attempted.

Procedure: CSF Diversion
CSF drainage

Active Comparator: Conventional CSF diversion

The EVD will be set to a level of 15 mmHg for as long as needed for the treatment of hydrocephalus, and subsequently weaned at the discretion of the treating physician. Lowering the level of the EVD can be considered by the treating physician if sustained intracranial hypertension occurs

Procedure: CSF Diversion
CSF drainage

Outcome Measures

Primary Outcome Measures

  1. Modified Rankin Scale [90-days]

    The primary outcome is clinical outcome at 90 days. A favorable outcome is defined as a score of 1 or 2 on the modified Rankin Score (mRS) and poor outcome defined as a mRS of 3-6. This assessment will be made by a clinician who was blinded to the patient's CSF diversion treatment arm.

Secondary Outcome Measures

  1. Infarction [90-days]

    Presence of radiologic infarction

  2. Vasospasm [90-days]

    Evidence of vasospams based upon TCD and/or angiography

  3. Shunt placement [90-days]

    Rate of shunt placement

  4. Ventriculitis [90-days]

    Rate of ventriculitis

  5. Modified Rankin Scale [Hospital discharge (average 3 weeks)]

    Modified rankin Scale upon discharge from the hospital

  6. MMSE [90-days]

    Cognitive status evaluated using the MMSE

  7. Length of ICU stay [Average 3 weeks]

    Evalute the average length of ICU stay for this patient population.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No

Inclusion Criteria

  • Age ≥ 18 years

  • Diagnosis of acute subarachnoid hemorrhage (SAH), confirmed with noncontrast head CT

  • SAH is suspected to be aneurysmal in source

  • Clinical management requires placement of EVD within 2 days of suspected time of hemorrhage

Exclusion Criteria

  • Age < 18 years

  • SAH of traumatic or non-aneurysmal etiology

  • Patients treated with lumbar drains

  • EVD placement ≥ 3 days after suspected time of hemorrhage

  • Known contraindication to induction of relative intracranial hypotension (e.g. acute subdural hematoma)

  • Pre-morbid mRS ≥ 3

  • EVD that is suboptimally placed by CT obtained after EVD placement (i.e. EVD not in the ventricular system)

Contacts and Locations

Locations

Site City State Country Postal Code
1 Mayo Clinic in Florida Jacksonville Florida United States 32224
2 Mayo Clinic in Rochester Rochester Minnesota United States 55905

Sponsors and Collaborators

  • Mayo Clinic

Investigators

  • Principal Investigator: Giuseppe Lanzino, MD, Mayo Clinic

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Giuseppe Lanzino, MD, Mayo Clinic
ClinicalTrials.gov Identifier:
NCT01420978
Other Study ID Numbers:
  • 11-002713
First Posted:
Aug 22, 2011
Last Update Posted:
May 14, 2013
Last Verified:
May 1, 2013
Additional relevant MeSH terms:

Study Results

No Results Posted as of May 14, 2013