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NCT03357562Terminated

MR Imaging of Lung in the Follow-up Assessment of Cystic Fibrosis

Source: ClinicalTrials.gov · Last updated 9 Jun 2026

Reason given: Target number of inclusion not reached

Brief summary (registry, in English)

The aim of the study is to assess the diagnostic sensitivity of MRI to detect changes in Helbich-Bhalla scoring over time in patients with cystic fibrosis

Status (registry)
Terminated
Study type
Interventional
Enrollment
212 (actual)
First submitted
15 Nov 2017
Start date
5 May 2018
Primary completion date
6 Mar 2025
Lead sponsor
University Hospital, Bordeaux
NCT number
NCT03357562

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Patients with previous pulmonary transplantation or planned for transplantation in the year following inclusion

Other

  • patients without any social security or health insurance
  • pregnant women
  • MRI contraindications:

Who the study is looking for

  • male or female children (age ≥ 8 y.o) and adult patient with a diagnosis of cystic fibrosis provided by genetic and swear test older than 8 years. Subgroups of patients will be defined according to:
    • age: younger or older 18y.o. We expect around 50% in different subgroups. In case of, we reach 50% in one of these groups, patient recruitment will continue for both groups until the expected number of patients in the study is reached.
    • brand name of magnet: Siemens, General Electric or Philips
  • new drugs use: association Ivacaftor/lumicaftor (OrkambiØ) or Ivacaftor only (Kalydeco Ø) ) We expect approximately 20% to 50% of patients treated
  • Informed consent provided to the patient or/and to legal representative for adults and to parents for the children
  • Patient concerned by articles L 1121-6, L 1121-7, and L 1121-8 (persons deprived of their liberty by a judicial or administrative decision, minors, persons of legal age who are the object of a legal protection measure or unable to express their consent) if the expected benefit for such persons justifies the foreseeable risk incurred

Age in the registry: 8 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (10)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
University Hospital of BordeauxBordeauxFranceUnknown status
Hopital Henri MondorCréteilFranceUnknown status
CHRU de GrenobleGrenobleFranceUnknown status
CHRU de LilleLilleFranceUnknown status
Hôpital NordMarseilleFranceUnknown status
Hopital Universitaire de la TimoneMarseilleFranceUnknown status
Fondation LenvalNiceFranceUnknown status
Hôpital Necker Enfant MaladesParisFranceUnknown status
Hôpital Armand-TrousseauParisFranceUnknown status
CHRU Bretonneau-ToursToursFranceUnknown status

Are you the coordinator? Confirm the details

This page is information, not medical advice. Discuss any trial with your doctor.