Standard clinical practice: The study will be carried out in the context of the usual clinical practice conditions, not imposing restrictions on the participating physician or influencing their normal clinical practice.
Study summary
REPTT is an observational, prospective, multi-country, multicentre and non-interventional registry in which at least 300 patients with Thrombotic thrombocytopenic purpura (TTP) in Spain and Portugal will be evaluated.
The study will be carried out in the context of the usual clinical practice conditions, not imposing restrictions on the participating physician or influencing their normal clinical practice.
Eligibility
Sex
ALL
Min age
—
Max age
99 Years
Healthy volunteers
No
Inclusion Criteria:
1. Patients with diagnosis of TTP according to International Consensus criteria from centres in Spain and Portugal.
2. Patients that voluntarily sign the informed consent. For subjects unable to provide informed consent, a fully recognized medical authority may be used according to local laws.
3. Patients between 0 to 99 years old at the time of diagnosis.
Note: Decision was taken to treat the patient with an specific treatment prior and independently of patient inclusion in this non interventional study.
Exclusion Criteria:
1. Inability to comply with study procedures and follow-up exams.
2. Patients with any type of alteration that compromises their ability to grant written informed consent.
3. Patients that do not consent to participate in the study and do not sign informed consent.
4. Patients that do not meet the criteria previously mentioned for TTP.
Primary outcome measure(s)
Incidence of TTP in Spain/Portugal — Throughout the study period, calculated for the 3 years of expected duration. Number of patients diagnosed with TTP and enrolled in the registry per year
Morbidity of TTP in Spain/Portugal — Throughout the study period, calculated for the 3 years of expected duration. Percentage of patients diagnosed with TTP and enrolled in the registry among spanish / portuguese population per year
Mortality of TTP in Spain/Portugal — Throughout the study period, calculated for the 3 years of expected duration. Percentage of patients diagnosed with TTP and enrolled in the registry per year who died due to the disease
Trial sites (7)
Facility
City
Region
Status
Hospital Universitario Virgen del Rocío
Seville
Andalusia
Recruiting
Hospital Universitario Bellvitge
L'Hospitalet de Llobregat
Barcelona
Recruiting
Hospital Clínic Barcelona
Barcelona
Spain
Recruiting
Hospital Universitario de Guadalajara
Guadalajara
Spain
Recruiting
Hospital Universitario La Paz
Madrid
Spain
Recruiting
Hospital Virgen de la Arrixaca
Murcia
Spain
Recruiting
Hospital Clínico Universitario de Valencia
Valencia
Spain
Recruiting
More Fundación Española de Hematología y Hemoterapía trials in Spain
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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