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RecruitingNCT07867834TEMPOUpdated Oct 9, 2026

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

An interventional study of TEMPO in Hemophilia, sponsored by Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico. Recruiting at 1 site in Italy. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-10-09.

Sponsored by Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico · Not applicable, Interventional, and Supportive care

From the registry’s dates

  • Registered 11 months after the study started (first participant enrolled Oct 2025, registered Oct 2026).
  • Started Oct 2025; still recruiting 1 year later.
Updated Oct 9, 2026Newly registeredGo to Updates ↓
Phase
Not applicable
Study type
Interventional
Enrollment
50
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

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.

02

Conditions studied

  • Hemophilia

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Keywords

  • Hemophilia
03

In context

Hemophilia A

885 studies on the registry are indexed under Hemophilia A; 139 are open to participants now.

This study's planned enrollment of 50 is above the median of 27 across 523 interventional studies indexed under Hemophilia A.

Browse Hemophilia A studies →

Lead sponsor

Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico is the lead sponsor of 232 studies on the registry; 83 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • informed consent
  • age (minimum 18 years)
  • hemophilia
  • having a smartphone

Exclusion criteria

Exclusion Criteria:

  • autoimmune, inflammatory or degenerative diseases that cause arthritis
05

Study design

Phase
Not applicable
Primary purpose
Supportive care
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
50 participants (estimated)

Study arms

  • Experimental
    TEMPO

    TEMPO system

    Other: TEMPO

  • No intervention
    CONTROL

    No intervention

Interventions

  • OtherTEMPO

    Personalized telemedicine

06

What researchers measure

Primary outcomes

  1. Veritas Pro score

    Score for adherence to prophylactic treatment

    Time frame: 6 months

07

Study locations

1 of 1 sites recruiting
  • Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico
    Milan, Italy
    Recruiting
08

Updates

1 registry update since Sep 25, 2026
Registered
First appeared on the registry. No changes since
Oct 9, 2026
Show all 1 update
  1. Oct 9, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

09

Registry details

Key details

Study ID
NCT07867834
Responsible party
Sponsor
First posted
Oct 9, 2026
Start date
Oct 19, 2025
Primary completion
Aug 31, 2026
Completion
Sep 30, 2026 (estimated)
Last update
Oct 9, 2026

Study contacts

Roberta Gualtierotti, Professor
Contact
roberta.gualtierotti@unimi.it
+39 0255034072

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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