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Multicenter Observational Ambispective Study for Congenital Platelet Disorders
Inherited platelet disorders (IPD) are a heterogeneous group of rare bleeding diseases associated with a reduction of platelet number and/or function and with a bleeding tendency ranging from mild to severe. The frequency of inherited thrombocytopenias has been estimated to be 2.7/100,000 while the prevalence of inherited platelet function disorders is unknown, partly because they are frequently overlooked due to their difficult diagnosis.
This a no-profit national multicenter ambispectic (retrospective and prospective) observational study. After collection of informed consent form each patient, each center will enroll the patient and will collect general, laboratory and clinical data on an electronic CRF on a REDCAP platform. Each patient will receive a unique identification number. All clinical events will be reported in the data base.
Age
All ages
Sex
ALL
Healthy Volunteers
No
Fondazione Policlinico Universitario A.Gemelli IRCCS
Roma, Roma, Italy
Fondazione Policlinico Universitario A.Gemelli IRCCS, Roma, Roma 00168
Rome, rome, Italy
Start Date
October 15, 2024
Primary Completion Date
October 1, 2028
Completion Date
October 30, 2028
Last Updated
November 15, 2024
200
ESTIMATED participants
Lead Sponsor
Fondazione Policlinico Universitario Agostino Gemelli IRCCS
NCT06414889
NCT06261060
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and ConditionsNCT05196789