Cranioplasty Cognitive Outcome Study
Primary Purpose
Cognitive Impairment, Brain Herniation
Status
Unknown status
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
"Early" cranioplasty
Sponsored by
About this trial
This is an interventional treatment trial for Cognitive Impairment focused on measuring Cranioplasty, Craniectomy, Cognitive impairment, Syndrome of the trephined
Eligibility Criteria
Inclusion Criteria:
- Age greater than or equal to 18 years-old,
- Craniectomy was performed due to head injury, infarct or spontaneous intracerebral hemorrhage, and benign tumors.
- Craniectomy skull defect size of >10cm at its longest diameter
- Craniectomy performed at any of the Hospital Authority's Neurosurgical Centers after 1st March 2019
Exclusion Criteria:
- Age older than 80 years-old,
- Patients cannot communicate by obeying simple command,
- Patients who are unfit for cranioplasty as decided by the treating neurosurgeon
- Posterior fossa craniectomy
- Craniectomy performed before 1st March 2019
- Craniectomy performed at an institution outside the Hospital Authority
- Any pre-existing illness that renders the patient moderately or severely disabled before the brain insult.
- Patients that need an additional procedure e.g. cerebrospinal fluid shunting with cranioplasty in the same setting.
- History of central nervous system infection
- Craniectomy-related complications such as hemorrhage or surgical site infection requiring surgical intervention or deemed to affect patient's long-term cognitive outcome
- Claustrophobia or any other medical condition that prohibits the patient from undergo MRI scanning
- Patients who cannot understand spoken English or Chinese
Sites / Locations
- Kwong Wah HospitalRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
No Intervention
Experimental
Arm Label
"Late" cranioplasty
"Early" cranioplasty
Arm Description
Subjects undergoing cranioplasty within 3 months after craniectomy.
Subjects undergoing cranioplasty beyond 3 months after craniectomy.
Outcomes
Primary Outcome Measures
Montreal Cognitive Assessment (MOCA)
Minimum (worse): 0/30; Maximum (best) 30/30. Higher values represent a better outcome.
Neurobehavioural Cognitive State Examination (NCSE)
Multi-domain assessment involving: orientation, attention, registration, comprehension, repetition, naming, construction, calculation, similarities,judgement. Stratification of each domain into mild, moderate and severe impairment. The higher the number the better the outcome.
Rivermead Behavioural Memory Test (RBMT)
Secondary Outcome Measures
Motor assessment
Medical Research Council limb power
Modified Functional Ambulation Category (MFAC)
7 ordinal scale assessment. The lower the scale, the worse the ambulatory ability of the patient. I: bed bound; 2: wheel-chair bound; 3: dependent walker; 4: Assisted walker; 5: Supervised walker; 6: Indoor walker; 7: Outdoor walker (patient can walk anywhere).
Quality of life assessment
Short Form-36 (SF-36)
Psychological assessment
Beck depression inventory (BDI)
Caregiver assessment
Caregiver Strain Index
Caregiver
Caregiver self-assessment questionnaire
MRI cerebral perfusion assessment
Cerebral blood flow
Full Information
NCT ID
NCT03791996
First Posted
December 30, 2018
Last Updated
October 15, 2019
Sponsor
Kwong Wah Hospital
Collaborators
The Queen Elizabeth Hospital, Queen Mary Hospital, Hong Kong, Prince of Wales Hospital, Shatin, Hong Kong, Princess Margaret Hospital, Canada, Tuen Mun Hospital, Pamela Youde Nethersole Eastern Hospital
1. Study Identification
Unique Protocol Identification Number
NCT03791996
Brief Title
Cranioplasty Cognitive Outcome Study
Official Title
Impact of Cranioplasty on Cognitive Outcome: A Multi-Center Prospective Randomized Study
Study Type
Interventional
2. Study Status
Record Verification Date
October 2019
Overall Recruitment Status
Unknown status
Study Start Date
March 1, 2019 (Actual)
Primary Completion Date
September 1, 2020 (Anticipated)
Study Completion Date
March 1, 2021 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Kwong Wah Hospital
Collaborators
The Queen Elizabeth Hospital, Queen Mary Hospital, Hong Kong, Prince of Wales Hospital, Shatin, Hong Kong, Princess Margaret Hospital, Canada, Tuen Mun Hospital, Pamela Youde Nethersole Eastern Hospital
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
This will be a multicenter prospective randomized study of adult patients with an acquired skull defect as a result of craniectomy and considered suitable for cranioplasty, i.e. reconstruction of the skull defect, at all seven Hong Kong Hospital Authority neurosurgical units. Patients that underwent their primary craniectomy operation at any of the Hospital Authority neurosurgery centers from the 1st March 2019 and considered suitable for cranioplasty will be included in this study. Those who underwent their primary craniectomy before 1st March 2019 or at an institution other than the aforementioned neurosurgical units will be excluded. Data from clinical records, operation notes, medication-dispensing records, laboratory records and radiological reports will be collected.
30 adult patients with craniectomy will be recruited and randomized into two groups: "early" cranioplasty, i.e. performed within 3 months of craniectomy, and "late", i.e. cranioplasty performed more than 3 months after the operation. The aim of the study is to determine whether early cranioplasty can improve on patient's cognitive performance compared to those who undergo the procedure after 3 months.
Detailed Description
Decompressive craniectomy, a neurosurgical procedure where a portion of the skull calvarium is removed, is a life-saving procedure. The complication rate of cranioplasty, a neurosurgical procedure where the acquired skull defect is reconstructed, ranges from 11% to 26% and includes postoperative hemorrhage and infection. (4) The syndrome of the trephined is a recognized long-term complication in which certain groups of patients, experience debilitating neurocognitive deficits in addition to chronic headache, dizziness, fatigability and clinical depression. (2) It is believed that the lack of an overlying bone may cause undue significant atmospheric pressure on the underlying cortex, thereby reducing cerebral perfusion and cerebrospinal fluid flow. There are reports that cognitive improvement can be observed in up to 30% of patients after cranioplasty yet the underlying mechanism for this observation is unclear. (1) Some studies have demonstrated enhanced cerebral perfusion by non-invasive investigations, but there is a lack of large scale systematically performed studies to verify such cerebral hemodynamic effects. (1-3) Clinical equipoise exists regarding the optimum timing of cranioplasty procedures after craniectomies. While the anecdotal practice of delaying cranioplasty for at least 3 months after a craniectomy is common, local and overseas observational studies suggest that performing early cranioplasties (i.e. within 3 months) is equally safe in terms of infection and other operative complications. (4-6)
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cognitive Impairment, Brain Herniation
Keywords
Cranioplasty, Craniectomy, Cognitive impairment, Syndrome of the trephined
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
2-arm randomised study with subjects centrally randomised by assigning them into either the control "late" cranioplasty group or the intervention "early" cranioplasty group.
All subjects will eventually receive the cranioplasty procedure.
Masking
None (Open Label)
Masking Description
1:1 block central randomisation with assignments written on a card sealed in an opaque envelop.
Allocation
Randomized
Enrollment
30 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
"Late" cranioplasty
Arm Type
No Intervention
Arm Description
Subjects undergoing cranioplasty within 3 months after craniectomy.
Arm Title
"Early" cranioplasty
Arm Type
Experimental
Arm Description
Subjects undergoing cranioplasty beyond 3 months after craniectomy.
Intervention Type
Procedure
Intervention Name(s)
"Early" cranioplasty
Intervention Description
Subjects undergoing cranioplasty beyond 3 months after craniectomy.
Primary Outcome Measure Information:
Title
Montreal Cognitive Assessment (MOCA)
Description
Minimum (worse): 0/30; Maximum (best) 30/30. Higher values represent a better outcome.
Time Frame
3-months
Title
Neurobehavioural Cognitive State Examination (NCSE)
Description
Multi-domain assessment involving: orientation, attention, registration, comprehension, repetition, naming, construction, calculation, similarities,judgement. Stratification of each domain into mild, moderate and severe impairment. The higher the number the better the outcome.
Time Frame
3-months
Title
Rivermead Behavioural Memory Test (RBMT)
Time Frame
3-months
Secondary Outcome Measure Information:
Title
Motor assessment
Description
Medical Research Council limb power
Time Frame
3-months
Title
Modified Functional Ambulation Category (MFAC)
Description
7 ordinal scale assessment. The lower the scale, the worse the ambulatory ability of the patient. I: bed bound; 2: wheel-chair bound; 3: dependent walker; 4: Assisted walker; 5: Supervised walker; 6: Indoor walker; 7: Outdoor walker (patient can walk anywhere).
Time Frame
3-months
Title
Quality of life assessment
Description
Short Form-36 (SF-36)
Time Frame
3-months
Title
Psychological assessment
Description
Beck depression inventory (BDI)
Time Frame
3-months
Title
Caregiver assessment
Description
Caregiver Strain Index
Time Frame
3-months
Title
Caregiver
Description
Caregiver self-assessment questionnaire
Time Frame
3-months
Title
MRI cerebral perfusion assessment
Description
Cerebral blood flow
Time Frame
3-months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
79 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Age greater than or equal to 18 years-old,
Craniectomy was performed due to head injury, infarct or spontaneous intracerebral hemorrhage, and benign tumors.
Craniectomy skull defect size of >10cm at its longest diameter
Craniectomy performed at any of the Hospital Authority's Neurosurgical Centers after 1st March 2019
Exclusion Criteria:
Age older than 80 years-old,
Patients cannot communicate by obeying simple command,
Patients who are unfit for cranioplasty as decided by the treating neurosurgeon
Posterior fossa craniectomy
Craniectomy performed before 1st March 2019
Craniectomy performed at an institution outside the Hospital Authority
Any pre-existing illness that renders the patient moderately or severely disabled before the brain insult.
Patients that need an additional procedure e.g. cerebrospinal fluid shunting with cranioplasty in the same setting.
History of central nervous system infection
Craniectomy-related complications such as hemorrhage or surgical site infection requiring surgical intervention or deemed to affect patient's long-term cognitive outcome
Claustrophobia or any other medical condition that prohibits the patient from undergo MRI scanning
Patients who cannot understand spoken English or Chinese
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Calvin Mak, MBBS FRCS
Phone
35066026
Email
mhk349@ha.org.hk
First Name & Middle Initial & Last Name or Official Title & Degree
Marina Lee
Phone
35066026
Email
leeymm@ha.org.hk
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Calvin Mak, MBBS FRCS
Organizational Affiliation
Neurosurgery, Queen Elizabeth Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Kwong Wah Hospital
City
Hong Kong
State/Province
Hong Kong
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Peter YM Woo, FRCS (SN)
Phone
852+ 3517 2275
Ext
2275
Email
peterymwoo@gmail.com
First Name & Middle Initial & Last Name & Degree
Peter YM Woo, FRCS (SN)
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
28368505
Citation
Halani SH, Chu JK, Malcolm JG, Rindler RS, Allen JW, Grossberg JA, Pradilla G, Ahmad FU. Effects of Cranioplasty on Cerebral Blood Flow Following Decompressive Craniectomy: A Systematic Review of the Literature. Neurosurgery. 2017 Aug 1;81(2):204-216. doi: 10.1093/neuros/nyx054.
Results Reference
background
PubMed Identifier
23662672
Citation
Bender A, Heulin S, Rohrer S, Mehrkens JH, Heidecke V, Straube A, Pfefferkorn T. Early cranioplasty may improve outcome in neurological patients with decompressive craniectomy. Brain Inj. 2013;27(9):1073-9. doi: 10.3109/02699052.2013.794972. Epub 2013 May 10.
Results Reference
result
PubMed Identifier
27489166
Citation
Ashayeri K, M Jackson E, Huang J, Brem H, Gordon CR. Syndrome of the Trephined: A Systematic Review. Neurosurgery. 2016 Oct;79(4):525-34. doi: 10.1227/NEU.0000000000001366.
Results Reference
result
PubMed Identifier
27499122
Citation
Malcolm JG, Rindler RS, Chu JK, Grossberg JA, Pradilla G, Ahmad FU. Complications following cranioplasty and relationship to timing: A systematic review and meta-analysis. J Clin Neurosci. 2016 Nov;33:39-51. doi: 10.1016/j.jocn.2016.04.017. Epub 2016 Aug 4.
Results Reference
result
PubMed Identifier
26056810
Citation
Xu H, Niu C, Fu X, Ding W, Ling S, Jiang X, Ji Y. Early cranioplasty vs. late cranioplasty for the treatment of cranial defect: A systematic review. Clin Neurol Neurosurg. 2015 Sep;136:33-40. doi: 10.1016/j.clineuro.2015.05.031. Epub 2015 May 29.
Results Reference
result
PubMed Identifier
25827865
Citation
Tsang AC, Hui VK, Lui WM, Leung GK. Complications of post-craniectomy cranioplasty: risk factor analysis and implications for treatment planning. J Clin Neurosci. 2015 May;22(5):834-7. doi: 10.1016/j.jocn.2014.11.021. Epub 2015 Mar 28.
Results Reference
result
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Cranioplasty Cognitive Outcome Study
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