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RECRUITING
NCT04680715
PHASE2

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

Sponsor: Centre Antoine Lacassagne

View on ClinicalTrials.gov

Summary

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.

Official title: Per-Operative Radiotherapy (RPO) by Papillon +TM in Localized Breast Cancer : Faisability and Toxicity Study

Key Details

Gender

FEMALE

Age Range

65 Years - Any

Study Type

INTERVENTIONAL

Enrollment

40

Start Date

2021-07-16

Completion Date

2028-06

Last Updated

2026-01-29

Healthy Volunteers

No

Interventions

RADIATION

Per-Operative Radiotherapy technique by Papillon +TM

20Gy Per-Operative Radiotherapy technique by Papillon +TM, on localized breast cancer

Locations (2)

Pôle Santé République

Clermont-Ferrand, France

Centre Antoine Lacassagne

Nice, France