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Found 4 clinical trials
Nivolumab and Ipilimumab in Treating Patients With Rare Tumors

: Endocrine carcinoma of pancreas and digestive tract.) (closed to accrual) Neuroendocrine carcinoma including carcinoid of the lung (closed to accrual 12/19/2017) Pheochromocytoma

gonadotrophin releasing hormone
bone scan
adenoid cystic carcinoma
neutrophil count
somatostatin
  • 6048 views
  • 24 Sep, 2021
  • 818 locations
Diagnosis of Pheochromocytoma

The goal of this study is to develop better methods of diagnosis, localization, and treatment for pheochromocytomas. These tumors, which usually arise from the adrenal glands, are often difficult to detect with current methods. Pheochromocytomas release chemicals called catecholamines, causing high blood pressure. Undetected, the tumors can lead to severe …

dopa
chromogranin a
pheochromocytoma
somatostatin
hypertension
  • 16 views
  • 05 Sep, 2021
  • 2 locations
Genetic Analysis of Pheochromocytomas Paragangliomas and Associated Conditions

Pheochromocytomas and paragangliomas are neural crest-derived tumors of the nervous system that are often inherited and genetically heterogeneous. Genetic screening is recommended for patients and their relatives, and can guide clinical decisions. However, a mutation is not found in all cases. The aims of this proposal are to: 1) to …

tumors of the nervous system
genetic analysis
adrenal pheochromocytoma
crest
paraganglioma
  • 116 views
  • 01 Sep, 2021
  • 1 location
Adrenal Tumors - Pathogenesis and Therapy

The pathogenesis of adrenal tumors is still not fully elucidated and the treatment options for malignant tumors are poor. The current study investigates different aspects of the pathogenesis of adrenal tumors and evaluates different therapeutic options in patients with adrenocortical carcinoma.

malignancy
adrenocortical carcinoma
carcinoma
cancer
adrenal neoplasm
  • 60 views
  • 09 Jun, 2021
  • 1 location