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Spots Global Cancer Trial Database for Hypercoagulation Screening in Cancer

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Trial Identification

Brief Title: Hypercoagulation Screening in Cancer

Official Title: Hypercoagulation Screening as Innovative Tool for Risk Assessment, Early Diagnosis and Prognosis in Cancer

Study ID: NCT02622815

Interventions

Study Description

Brief Summary: There is a complex, mutual relationship between cancer and thrombosis. Indeed, the tumor has the capacity to activate the hemostatic system and this leads to an increased thrombotic risk in cancer patients. Even in the absence of clinical manifestations, cancer patients are commonly characterized by hemostatic abnormalities, recognized only by laboratory testing, which define the 'hypercoagulable state'. Of interest, hypercoagulation has been repeatedly reported to be associated with tumor progression and poor prognosis in various carcinomas. On the other hand, thrombotic event can represent the first signal of the presence of an occult tumor. These findings suggest that the coagulant pathway might play a role in the preclinical phase of cancer. The investigators hypothesize that a persistent, subclinical activation of the hemostatic system in an otherwise healthy subject, may predispose not only to thrombosis, but also to tumor formation and spreading. A major problem in primary cancer prevention is the lack of effective predictive markers of the disease. The HYPERCAN is an ongoing prospective Italian multicenter study organized around two tightly-interconnected research programs aiming to: 1_the assessment of thrombotic markers as a tool for cancer risk prediction in two large populations of healthy subjects, i.e. a group of healthy blood donors of Bergamo and Milano Provinces and a subgroup of Moli-sani subjects of the Molise region; and 2_ the evaluation whether thrombotic markers and/or the occurrence of overt thrombosis (or disseminated intravascular coagulation) may be prognostic of cancer disease outcomes (i.e. overall survival, progression free survival in metastatic cancer, disease free survival in limited disease) in cancer patients with different types of solid tumors (i.e. breast, lung and gastrointestinal cancers). Therefore, the assessment of cancer risk occurrence in healthy individuals might be useful for anticipation of cancer diagnosis. In addition, the results of this study might help to evaluate whether thrombotic markers may be prognostic of cancer outcomes independently of the disease extension.

Detailed Description:

Eligibility

Minimum Age:

Eligible Ages: CHILD, ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Istituti Ospedalieri Bergamaschi S.r.l. - Policlinico San Marco, Osio Sotto, Bergamo, Italy

A.S.S.T. Bergamo Ovest, Treviglio, Bergamo, Italy

I.R.C.C.S. Istituto Neurologico Mediterraneo NEUROMED, Pozzilli, Isernia, Italy

Fondazione Humanitas per la Ricerca, Rozzano, Milan, Italy

Papa Giovanni XXIII Hospital - Oncology Unit, Bergamo, , Italy

Papa Giovanni XXIII Hospital - S.I.M.T., Bergamo, , Italy

Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, , Italy

ASL Roma 1 - ACO San Filippo Neri & San Giovanni Maria Addolorata Hospital, Rome, , Italy

Contact Details

Name: Anna Falanga, MD

Affiliation: A.O. Papa Giovanni XXIII - Recruiting

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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