Telemedicine takes on lymphoma: a 350-Patient trial
NCT ID NCT03336138
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looked at whether using telemedicine (remote doctor visits) can improve how aggressive lymphomas are managed. The main goal was to see if patients got the right amount of chemotherapy on time. 350 patients from 10 hospitals took part. The study compared telemedicine support to usual care.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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350 people
The number who actually took part.
- Started
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Jan 2012
- Finished
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Jan 2019
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 80 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Patient with a recent diffuse large B cell lymphoma (LBDGC), histologically proven, with treatment not started * a priori likely to be treated by rituximab, cyclophosphamide, doxorubicin, vincristine, and prednisolone every 21 days (R-CHOP21) for 8 cycles or rituximab, doxorubicin, cyclophosphamide, vindesine, bleomycin, and prednisone (R-ACVBP). * Index international prognosis (IPI) measurable (IPI-aa), adjusted for age. Any IPI-aa is eligible. * accepting the study Exclusion Criteria: * Patient with another type of lymphoma (including transformed follicular forms) * Patient having already started his treatment. * Life expectancy \<3 months. * Carcinologic history * Serum positive for HIV or hepatitis B virus (HBV).
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Bayonne Hospital
Bayonne, 64000, France
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Clinique Claude Bernard
Albi, 81000, France
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Clinique Marzet
Pau, 64000, France
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Clinique Saint Jean
Toulouse, 31000, France
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Hospital
Auch, 32000, France
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Hospital
Montauban, 82000, France
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Rodez Hospital
Rodez, 12000, France
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Tarbes Hospital
Tarbes, 65000, France
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University Hospital Bordeaux
Bordeaux, 33000, France
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University Hospital of Toulouse
Toulouse, France, France
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