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Hypopituitarism after Severe Traumatic Brain Injury, an observational study

Hypopituitarism after Severe Traumatic Brain Injury, an observational study - -

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON32099
Enrollment
60
Registered
2008-07-09
Start date
2008-10-21
Completion date
Unknown
Last updated
2024-05-13

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

Conditions

hypopituitarism loss of function of the pituitary gland

Interventions

None listed

Sponsors

Vrije Universiteit Medisch Centrum
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Men and women 18 to 70 years of age TBI (traumatic brain injury) in past GCS is known at admission CT or MRI has been made after admission Informed consent subject

Exclusion criteria

Exclusion criteria: Pregnancy Pre*existing hypopituitarism or risk factors for hypopituitarism Pre*existing neuro*psychological and/or physical deficit which makes taking part in study and following protocol impossible Corticosteroid use Alcohol abuse and/or drug use

Design outcomes

Primary

MeasureTime frame
Primary aims: 1- To investigate the prevalence of hypopituitarism in patients after traumatic brain injury. 2- To investigate the prevalence of osteoporosis in this TBI population.

Secondary

MeasureTime frame
Secondary aims: 3- To investigate possible prognostic factors for development of hypopituitarism after severe traumatic brain injury. 4- To compare physical and neuropsychological performance in patients with and without hypopituitarism after severe TBI. 5- To study bone mineral density in patients after severe traumatic brain injury and study separately the bone mineral density in patients with and without hypopituitarism after traumatic brain injury and compare this with the normal population.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)