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Lumbar Drainage in Subarachnoid Haemorrhage (LUMAS)

Primary Purpose

Subarachnoid Hemorrhage

Status
Completed
Phase
Phase 2
Locations
United Kingdom
Study Type
Interventional
Intervention
Lumbar Drain (Medtronic lumbar drainage system)
No lumbar drain
Sponsored by
The Leeds Teaching Hospitals NHS Trust
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Subarachnoid Hemorrhage focused on measuring Subarachnoid haemorrhage, Aneurysm, Cerebrospinal fluid drainage

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Aneurysmal subarachnoid haemorrhage.
  2. Recruitment prior to day three post-haemorrhage.
  3. Written informed consent or relative assent given.
  4. WFNS grade 1-3.
  5. Fisher grade 2, 3 and 4 (without space occupying haematoma) on initial CT scan.
  6. No intraventricular haemorrhage, space occupying haematoma or other contra-indication to lumbar puncture.

Exclusion Criteria:

  1. Non-aneurysmal subarachnoid haemorrhage.
  2. Delayed presentation / recruitment (after day three post-haemorrhage)
  3. Written informed consent or relative assent denied or unobtainable.
  4. WFNS grade 4 or 5.
  5. Fisher grade 1 on initial CT scan.
  6. Intraventricular haematoma obstructing ventricular outflow.
  7. Intracranial haematoma with mass effect.
  8. Bleeding diathesis.

Sites / Locations

  • Leeds General Infirmary

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Other

Arm Label

Study

Control

Arm Description

Insertion of lumbar drain

Normal clinical management without lumbar drain

Outcomes

Primary Outcome Measures

Incidence of delayed ischaemic neurological deficit

Secondary Outcome Measures

Modified Rankin Score
Incidence of cerebrospinal fluid shunting
Incidence of completed infarct secondary to delayed ischaemic neurological deficit
Incidence of cerebrospinal fluid infection secondary to lumbar drainage

Full Information

First Posted
February 11, 2009
Last Updated
February 22, 2011
Sponsor
The Leeds Teaching Hospitals NHS Trust
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1. Study Identification

Unique Protocol Identification Number
NCT00842049
Brief Title
Lumbar Drainage in Subarachnoid Haemorrhage
Acronym
LUMAS
Official Title
Lumbar Drainage of Cerebrospinal Fluid in Aneurysmal Subarachnoid Haemorrhage: A Prospective Randomised Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
February 2009
Overall Recruitment Status
Completed
Study Start Date
November 2006 (undefined)
Primary Completion Date
July 2010 (Actual)
Study Completion Date
July 2010 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
The Leeds Teaching Hospitals NHS Trust

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Subarachnoid haemorrhage affects approximately 8000 people per year in the UK. The average age of a patient with subarachnoid haemorrhage is 50 years, although it is often seen in younger people (25-45 years). Despite modern medicine, the death and disability rate remains high both from the initial bleed and from the associated complications such as vasospasm. This is characterised by neurological impairment seen following the bleed. Despite modern treatment this is still associated with a poor outcome. This has significant implications due to the long term intensive neuro-rehabilitation these patients will require. A recent study has shown that placing a small drain in the lower back following a subarachnoid haemorrhage may reduce the chance of vasospasm occurring and result in a better outcome. This trial was not optimally performed and so a trial is needed to look at this in more detail. The investigators have set up such a trial in our neurosurgical unit. If the investigators confirm that there is an improvement in patient outcome, it will change our practice in the future.
Detailed Description
All patients who present to our department with proven aneurysmal SAH and fit the inclusion criteria (see below) will be approached for inclusion into the trial. Written informed consent will be sought prior to recruitment into the study. Written assent from the patient's relatives will be sought in those cases where neurological impairment prevents written informed consent being obtained from the patient. The patient will subsequently be randomised into the control arm or the study arm of the trial. The control arm consists of normal therapeutic intervention, including external ventricular drainage if required for hydrocephalus. Those randomised to the therapeutic arm will have a lumbar drain inserted and set to drain CSF at 5 ml/hour. This will continue until CSF is no longer blood stained or until day 10 following insertion. Primary outcome measures: 1. Incidence of delayed ischaemic neurological deficit. This is defined as new neurological deficit and/or impairment of consciousness without other identifiable cause at least three days post haemorrhage. New impairment of consciousness is defined as a drop in the Glasgow Coma Score of 1 motor point or 2 verbal/eye opening points. Secondary outcome measures: Modified Rankin Score at day 10 post ictus and at 6 months. Severity of delayed neurological deficit and the development of a complete infarct. Incidence of cerebrospinal fluid infection secondary to lumbar drainage Special note: If a patient has presented greater than three days following the initial bleed, any neurological deficit present may be a delayed neurological deficit and thus must be excluded from the trial. Should the lumbar drain fall out prematurely the patient will be asked whether they wish to continue in the study and, if so, the lumbar drain will be reinserted and management will continue as before. Patients showing signs of lumbar drain infection will have the drain removed, a sample of CSF and the drain tip sent to the microbiology laboratory and appropriate antibiotic therapy instituted. The neurosurgical unit at Leeds General Infirmary treated 313 patients with acute subarachnoid haemorrhage in the three years 1997-2000. Of these 243 patients would have been suitable for this study on the basis of their admission clinical status. The power calculation was derived from the estimate that 40% of patients treated with standard therapy will develop clinical vasospasm. If the retrospective study showed a minimum of 20% improvement in its outcome variables then we expect to see the same improvement. For an 85% power this requires 105 patients in each arm. We expect this to take 3.5 years based on the number of eligible patients that present to our unit with a 60-70% recruitment rate (approximately 30 patients per year per arm).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Subarachnoid Hemorrhage
Keywords
Subarachnoid haemorrhage, Aneurysm, Cerebrospinal fluid drainage

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
210 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Study
Arm Type
Experimental
Arm Description
Insertion of lumbar drain
Arm Title
Control
Arm Type
Other
Arm Description
Normal clinical management without lumbar drain
Intervention Type
Device
Intervention Name(s)
Lumbar Drain (Medtronic lumbar drainage system)
Other Intervention Name(s)
Medtronic lumbar drainage system
Intervention Description
Insertion of lumbar drain to drain cerebrospinal fluid
Intervention Type
Other
Intervention Name(s)
No lumbar drain
Intervention Description
No lumbar drain
Primary Outcome Measure Information:
Title
Incidence of delayed ischaemic neurological deficit
Time Frame
Within 21 days of haemorrhagic ictus
Secondary Outcome Measure Information:
Title
Modified Rankin Score
Time Frame
10 days and 6 months following haemorrhagic ictus
Title
Incidence of cerebrospinal fluid shunting
Time Frame
Within 12 months of haemorrhagic ictus
Title
Incidence of completed infarct secondary to delayed ischaemic neurological deficit
Time Frame
Within 21 days of ictus
Title
Incidence of cerebrospinal fluid infection secondary to lumbar drainage
Time Frame
Within 8 weeks of removal of lumbar drain

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Aneurysmal subarachnoid haemorrhage. Recruitment prior to day three post-haemorrhage. Written informed consent or relative assent given. WFNS grade 1-3. Fisher grade 2, 3 and 4 (without space occupying haematoma) on initial CT scan. No intraventricular haemorrhage, space occupying haematoma or other contra-indication to lumbar puncture. Exclusion Criteria: Non-aneurysmal subarachnoid haemorrhage. Delayed presentation / recruitment (after day three post-haemorrhage) Written informed consent or relative assent denied or unobtainable. WFNS grade 4 or 5. Fisher grade 1 on initial CT scan. Intraventricular haematoma obstructing ventricular outflow. Intracranial haematoma with mass effect. Bleeding diathesis.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Yahia Al-Tamimi, MCChB(Hons)
Organizational Affiliation
Leeds Teaching Hospital NHS Trust
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Stuart Ross, FRCS(SN)
Organizational Affiliation
Leeds Teaching Hospital NHS Trust
Official's Role
Study Director
Facility Information:
Facility Name
Leeds General Infirmary
City
Leeds
State/Province
West Yorkshire
ZIP/Postal Code
LS1 3EX
Country
United Kingdom

12. IPD Sharing Statement

Citations:
PubMed Identifier
15086227
Citation
Klimo P Jr, Kestle JR, MacDonald JD, Schmidt RH. Marked reduction of cerebral vasospasm with lumbar drainage of cerebrospinal fluid after subarachnoid hemorrhage. J Neurosurg. 2004 Feb;100(2):215-24. doi: 10.3171/jns.2004.100.2.0215.
Results Reference
background
PubMed Identifier
22282887
Citation
Al-Tamimi YZ, Bhargava D, Feltbower RG, Hall G, Goddard AJ, Quinn AC, Ross SA. Lumbar drainage of cerebrospinal fluid after aneurysmal subarachnoid hemorrhage: a prospective, randomized, controlled trial (LUMAS). Stroke. 2012 Mar;43(3):677-82. doi: 10.1161/STROKEAHA.111.625731. Epub 2012 Jan 26.
Results Reference
derived

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Lumbar Drainage in Subarachnoid Haemorrhage

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