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Taking people in ItalyNo phase

Telemedicine Monitoring for People With Hemophilia

Tests a telemedicine program to monitor treatment and bleeding in adults with hemophilia.

Plain-language title generated from the registry record
Registry title: Tight Control of Treatment Adherence and Efficacy by Telemedicine for an Improved Personalized Management of Patients With Hemophilia

Key facts

Where
Milan, ItalySee the site

Where in Italy

  • Fondazione IRCCS Cà Granda Ospedale Maggiore PoliclinicoMilan, ItalyTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
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Trial details

Who runs it
Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico
Trial code
NCT07867834
Record updated
9 October 2026
Original description
In patients with haemophilia, close monitoring of bleeding with optimal adherence to treatment, a personalised treatment programme and the possibility of early diagnosis of haemarthrosis are essential. The TEMPO project will help advance the state of the art in optimal adherence, rigorous monitoring, and accurate and early diagnosis and management of haemarthrosis by collecting and integrating big data in order to personalise the treatment regimen for each patient, as envisaged by the current model of personalised medicine.Read full original descriptionShow less

Tight Control of Treatment Adherence and Efficacy by Telemedicine for an Improved Personalized Management of Patients With Hemophilia

In patients with haemophilia, close monitoring of bleeding with optimal adherence to treatment, a personalised treatment programme and the possibility of early diagnosis of haemarthrosis are essential. The TEMPO project will help advance the state of the art in optimal adherence, rigorous monitoring, and accurate and early diagnosis and management of haemarthrosis by collecting and integrating big data in order to personalise the treatment regimen for each patient, as envisaged by the current model of personalised medicine.

Inclusion: informed consent; age (minimum 18 years); hemophilia; having a smartphone.

Exclusion: autoimmune, inflammatory or degenerative diseases that cause arthritis.

ClinicalTrials.gov NCT07867834