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NCT01101711 Clinical Trial

Endocrine Dysfunction and Quality of Life After Subarachnoid Hemorrhage

Quality of Life Clinical Trial

Official title:
Endocrine Dysfunction and Quality of Life After Subarachnoid Hemorrhage

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT01101711
Other study ID # 65/2006
Secondary ID
Status Completed
Phase N/A
First received April 8, 2010
Last updated September 6, 2012
Start date November 2006
Est. completion date September 2012

Study information
Verified date September 2012
Source Lund University Hospital
Contact n/a
Is FDA regulated No
Health authority Sweden: Swedish National Council on Medical Ethics
Study type Observational

Clinical Trial 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.

Recruitment information / eligibility
Status Completed
Enrollment 50
Est. completion date September 2012
Est. primary completion date February 2011
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- acute aneurysmal subarachnoid hemorrhage

Exclusion Criteria:

- unable to give informed consent

Study Design

Observational Model: Cohort, Time Perspective: Prospective

Related Conditions & MeSH terms

Locations
Country Name City State
Sweden Department of Neurosurgery Lund

Sponsors (1)
Lead Sponsor Collaborator
Lund University Hospital

Country where clinical trial is conducted

Sweden, 

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