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Endocrine Dysfunction and Quality of Life After Subarachnoid Hemorrhage

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ClinicalTrials.gov Identifier: NCT01101711
Recruitment Status : Completed
First Posted : April 12, 2010
Last Update Posted : September 7, 2012
Sponsor:
Information provided by (Responsible Party):
Erik Kronvall, Lund University Hospital

Brief Summary:
Investigation of the incidence of endocrine dysfunction following subarachnoid hemorrhage (SAH), and to see if this has a relation to CNS lesions as evaluated by MRI and to common symptoms after SAH such as general exhaustion, lack of initiative, increased sleep demand and reduced quality of life.

Condition or disease
Endocrine Dysfunction Cerebral Infarctions Quality of Life

Study Type : Observational
Estimated Enrollment : 50 participants
Observational Model: Cohort
Time Perspective: Prospective
Official Title: Endocrine Dysfunction and Quality of Life After Subarachnoid Hemorrhage
Study Start Date : November 2006
Actual Primary Completion Date : February 2011
Actual Study Completion Date : September 2012

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Bleeding
U.S. FDA Resources

Group/Cohort
Patients with subarachnoid hemorrhage



Biospecimen Retention:   None Retained
Blood and urine samples


Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
Patients from the southern part of Sweden who have suffered subarachnoid hemorrhage and admitted to the Department of Neurosurgery in Lund
Criteria

Inclusion Criteria:

  • acute aneurysmal subarachnoid hemorrhage

Exclusion Criteria:

  • unable to give informed consent

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01101711


Locations
Sweden
Department of Neurosurgery
Lund, Sweden
Sponsors and Collaborators
Lund University Hospital

Responsible Party: Erik Kronvall, Dr., Lund University Hospital
ClinicalTrials.gov Identifier: NCT01101711     History of Changes
Other Study ID Numbers: 65/2006
First Posted: April 12, 2010    Key Record Dates
Last Update Posted: September 7, 2012
Last Verified: September 2012

Additional relevant MeSH terms:
Infarction
Hemorrhage
Subarachnoid Hemorrhage
Cerebral Infarction
Ischemia
Pathologic Processes
Necrosis
Intracranial Hemorrhages
Cerebrovascular Disorders
Brain Diseases
Central Nervous System Diseases
Nervous System Diseases
Vascular Diseases
Cardiovascular Diseases
Brain Infarction
Brain Ischemia
Stroke