Menu
Peptide Database
Results
No peptides found
Featured

Use search to browse all 100+ peptides

IGF-1

Insulin-like Growth Factor 1, Somatomedin C

Quick Stats
Studies 92
Trials 100
Unknown OBSERVATIONAL NCT02915380

Pituitary Dysfunction After Aneurysmal Subarachnoid Hemorrhage

View on ClinicalTrials.gov Updated Dec 15, 2025

Brief Summary

Recently, the occurrence and potential impact of pituitary dysfunction after aSAH has gained increasing interest. Several studies have demonstrated pituitary dysfunction after SAH suggesting that pituitary dysfunction may be a contributing factor for residual symptoms after SAH. This is an observational multicentric study aimed to test the prevalence of thyroid abnormalities, other neuroendocrinological dysfunction and their influence on outcome of patients affected by aSAH.

Detailed Description

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 injury secondary insults as well as neurorehabilitation interventions. Recently, the occurrence and potential impact of pituitary dysfunction after aSAH has gained increasing interest. Several studies have demonstrated pituitary dysfunction after SAH suggesting that pituitary dysfunction may be a contributing factor for residual symptoms after SAH. However, questions remain about the real prevalence and impact of such dysfunction on patients' outcome both in the acute and chronic phase after these events. In two recent metanalysis, the prevalence of total pituitary dysfunction was found with pooled frequencies of 0.31 (95% confidence interval CI: 0.22-0.43) \[Can et a.\] and 49.3.0% (95% CI 41.6%-56.9%) \[Robba et al\] during the acute phase (\< 6 months from aSAH) and decreasing in the chronic phase to 0.25 (95% CI: 0.16-0.36) \[Can et al.\] and 25.6% (95% CI 18.0%-35.1%) \[Robba et al\]. However, the authors found high heterogenicity and different results between the available literature; many differences were found in the in the choice of time of pituitary function assessment and SAH, of diagnostic criteria and units of measurement used to establish the diagnosis of hypopituitarism after SAH. Finally, it is not clear which is the hormone axis more likely to be affected after aSAH. It is believed that, among the other, the incidence of thyroid dysfunction is the most relevant, as it is associated with severe clinical impairment and symptoms. In literature, the prevalence of thyroid dysfunction after aSAH is reported from 0 to 35%.\[Karaka, Tanrivedi\]. Hypothyroidism includes a wide variety of symptoms including weakness, fatigue, depression, irritability, memory loss and decreased libido. Should these abnormalities complicate more than one third of the patients, hormone testing and eventually replacement should become "standard of care" to test. In order to define the actual incidence of these abnormalities, an observational multicentric study to test thyroid abnormalities, including TSH, fT4 (free thyroxine) and fT3 (free triiodothyronine) changes, is warranted. Secondary endpoints of such study include the prevalence of other neuroendocrinological dysfunction and their influence on the patients' outcome.

Interventions

Name: Evaluation of pituitary endocrine function
Type: BIOLOGICAL
Description: The basal thyroid hormone and test to perform will be: TSH, fT4, fT3. When available, the following hormones will be tested: FSH, LH, estradiol (in women), testosterone (in men), sex hormone-binding globulin (SHBG), ACTH, cortisol, prolactin, Na, K; serum levels of GH and IGF-1; and serum and urine osmolality. Adrenal function will be evaluated through ACTH-stimulation testing . Adrenal or GH insufficiency will be evaluated by insulin tolerance testing (ITT)
Name: Evaluation of clinical outcome
Type: BEHAVIORAL
Description: Patients' outcome will be assessed as modified Rankin Scale (mRS) at discharge from the hospital, at 3, 6 and 12 months.
Name: Evaluation of neuropsychological function
Type: BEHAVIORAL
Description: Neuropsychological examination will be conducted focusing on verbal comprehension (Token Test) and visual neglect. Verbal and visual short term and working memory visuospatial construction and figural memory will be performed through Rey Osterrieth Complex figure test, and psychomotor speed attention and concentration through Trail Making Test.

Primary Outcomes

Measure: Incidence of thyroid disfunction
TimeFrame: At 2 weeks after aSAH
Description: Thyroid-stimulating hormone (TSH), free thyroxin (fT4), free triiodothyronine (fT3).
Measure: Incidence of thyroid disfunction
TimeFrame: 3 months after aSAH
Description: Thyroid-stimulating hormone (TSH), free thyroxin (fT4), free triiodothyronine (fT3).
Measure: Incidence of thyroid disfunction
TimeFrame: 6 months after aSAH
Description: Thyroid-stimulating hormone (TSH), free thyroxin (fT4), free triiodothyronine (fT3).
Measure: Incidence of thyroid disfunction
TimeFrame: 12 months after aSAH
Description: Thyroid-stimulating hormone (TSH), free thyroxin (fT4), free triiodothyronine (fT3).

Trial Information

NCT ID

NCT02915380

Status

Unknown

Study Type

OBSERVATIONAL

Sponsor

Dr. Rita Bertuetti

Last Updated

December 15, 2025

Related Peptides