The PIT-TBI Pilot Study
Primary Purpose
Pituitary Disorders, Traumatic Brain Injury
Status
Unknown status
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Pituitary function evaluation
Sponsored by
About this trial
This is an interventional other trial for Pituitary Disorders focused on measuring Pituitary Disorders, Traumatic Brain Injury, Critical Care, Outcome Research, Risk Factors, Patient Oriented Research
Eligibility Criteria
Inclusion Criteria:
- Adult (≥ 18 years old)
- Severe or moderate blunt TBI admitted to the ICU with a Glasgow Coma Scale ≤ 12 following initial resuscitation
Exclusion Criteria:
- Previously diagnosed or suspected pituitary disorder or disease
- Pregnant or lactating woman
- Penetrating TBI
- Solid malignancy with life expectation <12 months
- Liver Cirrhosis Child C
- Chronic Heart Failure (New York Heart Association class IV)
- End-stage chronic respiratory disease (O2 dependent)
- End-stage renal disease (chronic dialysis or to be expected)
- Neurological conditions influencing functional status (e.g. spinal cord injury, neuromuscular disease, dementia, prior TBI or stroke)
- No fixed address
- Physician refusal
- Brain death
- Unable to return to the study center to attend the follow-up visits
- Admission to the Intensive Care Unit of the participating center > 24 hours after TBI
Sites / Locations
- The Ottawa Hospital
- Sunnybrook Health Sciences Centre
- Hôpital du Sacré-Coeur de Montréal
- CHU de Sherbrooke - Hôpital Fleurimont
- CHU de Québec - Hôpital de l'Enfant-Jésus
Arms of the Study
Arm 1
Arm Type
Other
Arm Label
Pituitary function evaluation
Arm Description
Exams performed according to a determined schedule following admission in the intensive care unit in order to determine the risk factors and the outcome associated with pituitary disorders.
Outcomes
Primary Outcome Measures
Adherence to the Protocol
Percentage of participants who underwent pituitary function evaluation and outcome measures as detailed in the Assigned Interventions section
Enrollment Rate
Number of patients recruited per month per site
Secondary Outcome Measures
Neurological Recovery
Glasgow Outcome Scale Extended (GOSe)
Quality of life
EuroQuol - EQ-5D-5L questionnaire
Independent functioning
Functional Independence Measure (FIM) questionnaire
Depression
Patient Health Questionnaire (PHQ-9)
Life satisfaction
Life Satisfaction Questionnaire (LISAT)
Secondary hypothyroidism
Secondary hypogonadism
Secondary adrenal insufficiency
Growth hormone deficit
Full Information
NCT ID
NCT02480985
First Posted
June 18, 2015
Last Updated
March 24, 2017
Sponsor
CHU de Quebec-Universite Laval
Collaborators
Canadian Institutes of Health Research (CIHR), Canadian Critical Care Trials Group, Fonds de la Recherche en Santé du Québec
1. Study Identification
Unique Protocol Identification Number
NCT02480985
Brief Title
The PIT-TBI Pilot Study
Official Title
Clinical Outcomes and Predictors of PITuitary Disorders in Patients With Moderate and Severe Traumatic Brain Injury: the PIT-TBI Prospective Multicenter Pilot Cohort Study
Study Type
Interventional
2. Study Status
Record Verification Date
March 2017
Overall Recruitment Status
Unknown status
Study Start Date
March 2015 (undefined)
Primary Completion Date
March 2018 (Anticipated)
Study Completion Date
March 2018 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
CHU de Quebec-Universite Laval
Collaborators
Canadian Institutes of Health Research (CIHR), Canadian Critical Care Trials Group, Fonds de la Recherche en Santé du Québec
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Damage to the pituitary gland is a frequently overlooked but potentially important complication of traumatic brain injury (TBI). Disorders of the pituitary gland can cause dysfunction of the thyroid, adrenals, ovaries and testes. These disorders may occur immediately or several months after TBI, may delay recovery and may have a significant negative impact on quality of life. TBI is the leading cause of disability and major permanent functional impairment among adults under 45 years of age. Hormonal deficits may contribute to common symptoms experienced by TBI survivors such as fatigue, poor concentration, depression and low exercise capacity. However, the association between hormonal deficits and disability remains uncertain. The primary objective of this pilot study is to assess the feasibility of a larger study that will evaluate the impact of pituitary disorders on neurological disability and functional recovery. The results of this study will provide key findings in the impact of pituitary disorders following TBI, which is a mandatory step prior testing the effect of hormonal replacement therapy in this population in costly clinical trials. If no relationship between pituitary disorders and disability is observed, the investigators' findings will prevent unnecessary, time-consuming and costly hormonal screening and will discourage potentially harmful hormonal therapy.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pituitary Disorders, Traumatic Brain Injury
Keywords
Pituitary Disorders, Traumatic Brain Injury, Critical Care, Outcome Research, Risk Factors, Patient Oriented Research
7. Study Design
Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
70 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Pituitary function evaluation
Arm Type
Other
Arm Description
Exams performed according to a determined schedule following admission in the intensive care unit in order to determine the risk factors and the outcome associated with pituitary disorders.
Intervention Type
Other
Intervention Name(s)
Pituitary function evaluation
Intervention Description
Pituitary function evaluation performed at hospital discharge, 6 and 12 months
Thyroid-stimulating hormone, free T4 and T3
Follicle stimulating hormone, luteinizing hormone, estradiol, bioavailable testosterone
Adrenocorticotropic hormone stimulation test
Glucagon test (growth hormone deficit)
Risk factors evaluation of pituitary dysfunction
Demographic data
Daily data (clinical exam, secondary brain injuries)
Hormone levels on day 1, 3 and 7
Biomarkers on day 1, 3 and 7
Brain CT-Scan on day 1
Pituitary MRI on day 7
Outcome measures at 6 and 12 months
Neurological recovery (GOSe)
Independent functioning (FIM)
Quality of life (EQ-5D-5L)
Life satisfaction (LISAT-11)
Depression (PHQ-9)
Primary Outcome Measure Information:
Title
Adherence to the Protocol
Description
Percentage of participants who underwent pituitary function evaluation and outcome measures as detailed in the Assigned Interventions section
Time Frame
12 months
Title
Enrollment Rate
Description
Number of patients recruited per month per site
Time Frame
12 months
Secondary Outcome Measure Information:
Title
Neurological Recovery
Description
Glasgow Outcome Scale Extended (GOSe)
Time Frame
12 months
Title
Quality of life
Description
EuroQuol - EQ-5D-5L questionnaire
Time Frame
12 months
Title
Independent functioning
Description
Functional Independence Measure (FIM) questionnaire
Time Frame
12 months
Title
Depression
Description
Patient Health Questionnaire (PHQ-9)
Time Frame
12 months
Title
Life satisfaction
Description
Life Satisfaction Questionnaire (LISAT)
Time Frame
12 months
Title
Secondary hypothyroidism
Time Frame
12 months
Title
Secondary hypogonadism
Time Frame
12 months
Title
Secondary adrenal insufficiency
Time Frame
12 months
Title
Growth hormone deficit
Time Frame
12 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Adult (≥ 18 years old)
Severe or moderate blunt TBI admitted to the ICU with a Glasgow Coma Scale ≤ 12 following initial resuscitation
Exclusion Criteria:
Previously diagnosed or suspected pituitary disorder or disease
Pregnant or lactating woman
Penetrating TBI
Solid malignancy with life expectation <12 months
Liver Cirrhosis Child C
Chronic Heart Failure (New York Heart Association class IV)
End-stage chronic respiratory disease (O2 dependent)
End-stage renal disease (chronic dialysis or to be expected)
Neurological conditions influencing functional status (e.g. spinal cord injury, neuromuscular disease, dementia, prior TBI or stroke)
No fixed address
Physician refusal
Brain death
Unable to return to the study center to attend the follow-up visits
Admission to the Intensive Care Unit of the participating center > 24 hours after TBI
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
François Lauzier, MD MSc FRCPC
Organizational Affiliation
CHU de Quebec Research Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
The Ottawa Hospital
City
Ottawa
State/Province
Ontario
Country
Canada
Facility Name
Sunnybrook Health Sciences Centre
City
Toronto
State/Province
Ontario
Country
Canada
Facility Name
Hôpital du Sacré-Coeur de Montréal
City
Montreal
State/Province
Quebec
Country
Canada
Facility Name
CHU de Sherbrooke - Hôpital Fleurimont
City
Sherbrooke
State/Province
Quebec
Country
Canada
Facility Name
CHU de Québec - Hôpital de l'Enfant-Jésus
City
Quebec
Country
Canada
12. IPD Sharing Statement
Citations:
PubMed Identifier
24247474
Citation
Lauzier F, Turgeon AF, Boutin A, Shemilt M, Cote I, Lachance O, Archambault PM, Lamontagne F, Moore L, Bernard F, Gagnon C, Cook D. Clinical outcomes, predictors, and prevalence of anterior pituitary disorders following traumatic brain injury: a systematic review. Crit Care Med. 2014 Mar;42(3):712-21. doi: 10.1097/CCM.0000000000000046.
Results Reference
background
Links:
URL
http://www.ccctg.ca
Description
Related Info
URL
http://www.criticalcare-neurotrauma.ca
Description
Related Info
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The PIT-TBI Pilot Study
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