EligibleTrials

Per-Operative Radiotherapy by Papillon +TM in Localized Breast Cancer

Recruiting · NCT04680715 · Interventional (participants receive a specific treatment)

View the official record on ClinicalTrials.gov →
Breast cancer

Interventions studied

Per-Operative Radiotherapy technique by Papillon +TM

What this trial is about

Phase II study; open recruitment, multicentrique. The aim of this clinical research is to evaluate faisability and toxicity of the per-operative radiotherapy using PAPILLON + TM device for localized breast cancers patients over 65 years.

Who can take part

Age range
65 Years and older
Sex
Female
Healthy volunteers
No - a diagnosis or condition is required
Phase
Phase 2
Study type
Interventional (participants receive a specific treatment)

Inclusion criteria

Exclusion criteria

Where it is running

2 locations listed.

Read the full protocol, contacts and eligibility on ClinicalTrials.gov →

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