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Search / Trial NCT02915380

Pituitary Dysfunction After Aneurysmal Subarachnoid Hemorrhage

Launched by DR. RITA BERTUETTI · Sep 23, 2016

Trial Information

Current as of July 21, 2025

Unknown status

Keywords

ClinConnect Summary

The incidence of aneurysmal subarachnoid hemorrhage (aSAH) varies between 6 to 10/100,000 subjects per year and it is a major cause of death and disability. The mortality rate ranges from 40 to 50%, and those who do survive SAH have high rates of functional limitations that could lead to impaired quality of life, including fatigue, depression, and loss of motivation.

Because aSAH affects patients in their most productive years of life, the disease has important social, and economic implications, and early prediction of long-term outcome is based on multiple factors including the primary in...

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • patients with acute aneurysmal SAH aged between 18 and 70 years of age who could be subjected to endocrine evaluation within 10 days of ictus and at follow-up.
  • Exclusion Criteria:
  • be major depression, psychiatric premorbidity, pituitary adenoma or perisellar lesion,preexisting hypopituitarism of any degree, previous hormonal substitution, patients in moribund state, pregnancy, glucocorticoid medication on admission to hospital or during treatment, prior pituitary insufficiency, and unsalvageable aSAH.

About Dr. Rita Bertuetti

Dr. Rita Bertuetti is a distinguished clinical trial sponsor with extensive experience in the design and management of innovative research studies. With a strong background in clinical medicine and a commitment to advancing healthcare, Dr. Bertuetti leads initiatives that prioritize patient safety and scientific integrity. Her expertise encompasses a wide range of therapeutic areas, and she is dedicated to fostering collaborative partnerships with academic institutions and industry stakeholders. Through her leadership, Dr. Bertuetti aims to drive impactful clinical research that translates into meaningful improvements in patient outcomes.

Locations

Patients applied

0 patients applied

Trial Officials

Chiara Robba, MD

Study Director

Cambridge University Hospitals NHS Foundation Trust

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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