Actively Recruiting

Phase 2
Age: 18Years +
All Genders
NCT05653635

Contribution From PET-DOPA in Glioblastoma Re-irradiation - A Randomized Phase II Study

Led by Centre Paul Strauss · Updated on 2026-02-04

54

Participants Needed

2

Research Sites

130 weeks

Total Duration

On this page

Sponsors

C

Centre Paul Strauss

Lead Sponsor

C

Centre Georges François Leclerc

Collaborating Sponsor

AI-Summary

What this Trial Is About

ReciDOPA is a phase II, single-stage randomized, multicenter, prospective trial assessing the efficacy of an irradiation protocol based on Intensity-modulated radiation therapy with simultaneous-integrated boost guided by FDOPA-PET in patient with recurrent glioblastoma.

CONDITIONS

Official Title

Contribution From PET-DOPA in Glioblastoma Re-irradiation - A Randomized Phase II Study

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age > 18 years
  • Glioblastoma, World Health Organization (WHO) grade IV, histologically proven
  • Performance status 0, 1 or 2
  • Neurological status 2 2
  • Past irradiation in previsional re-irradiated site or in the vicinity (5 to 7 cm)
  • Radiological proven recurrence according to 1 and 2 criteria, Wen et al
  • Remaining node after partial surgery post-recurrence
  • 1 to 3 recurrence site(s) < 35 mm in wide axis and separated by at least 5 mm
  • Volume of each lesion < 35 mL
  • Distance between recurrence node(s) and optic nerves (left and right), chiasma and/or cerebral trunk > 10 mm
Not Eligible

You will not qualify if you...

  • Patient with contraindication to MRI or PET
  • Glioblastomatose
  • Pregnancy or breastfeeding
  • Patient that do not understand French
  • Patient without affiliation to the national or local social security
  • Patients not able to comply to the protocol assessments for geographic, social or psychological reasons
  • Minor or patients placed under guardianship or supervision
  • Patients deprived of liberty
  • Patients placed under judicial protection
  • Patients that are not able to express their consent

AI-Screening

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Trial Site Locations

Total: 2 locations

1

CHRU de Nancy

Nancy, De, France, 5400

Not Yet Recruiting

2

Centre Paul Strauss

Strasbourg, France, 67033

Actively Recruiting

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Research Team

A

Anne ANTHONY

CONTACT

M

MANON VOEGELIN

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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