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NCT00435006 Clinical Trial

Hypopituitarism Following Traumatic Brain Injury or Spontaneous Subarachnoidal Haemorrhages

Brain Injuries Clinical Trial

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT00435006
Other study ID # KF-01-107/03
Secondary ID
Status Completed
Phase N/A
First received February 13, 2007
Last updated February 13, 2007
Start date August 2003
Est. completion date June 2006

Study information
Verified date February 2007
Source Rigshospitalet, Denmark
Contact n/a
Is FDA regulated No
Health authority Denmark: The Danish National Committee on Biomedical Research Ethics
Study type Observational

Clinical Trial Summary

The purpose of this study is to assess the prevalence and predictors of pituitary dysfunction, as well as secondary out-come in patients with traumatic brain injury or spontaneous subarachnoidal haemorrhages.

Recruitment information / eligibility
Status Completed
Enrollment 0
Est. completion date June 2006
Est. primary completion date
Accepts healthy volunteers
Gender Both
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria:

- Clinical diagnosis of traumatic brain injury (TBI) or subarachnoidal haemorrhages (SAH)

Exclusion Criteria:

- Alcohol or drug abuse

- Prior TBI or SAH

- Chronic use of glucocorticoids

- Pregnancy or breast feeding

- Diagnosis of psychiatric diseases or malignant neoplasms

Study Design

Observational Model: Defined Population, Time Perspective: Longitudinal

Related Conditions & MeSH terms

Locations
Country Name City State
Denmark Dept. of Endocrinology PE2131, Copenhagen University Hospital, Rigshospitalet Copenhagen

Sponsors (4)
Lead Sponsor Collaborator
Rigshospitalet, Denmark AP Moeller Foundation, Novo Nordisk A/S, University of Copenhagen

Country where clinical trial is conducted

Denmark, 

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