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NCT07885410Recruiting

PERCE-MUCO: Perceptions and Expectations of People With Cystic Fibrosis Regarding a Change in Treatment

Perceptions and Expectations of Patients Regarding a Change in Treatment in Cystic Fibrosis (PERCE-MUCO)

Source: ClinicalTrials.gov · Last updated 28 Oct 2026

Brief summary (registry, in English)

PERCE-MUCO is a prospective, multicentre, mixed-methods observational study investigating the perceptions, expectations and treatment-change intentions of adults with cystic fibrosis who are currently treated with elexacaftor/tezacaftor/ivacaftor (ETI) or whose treatment has been medically discontinued. The study focuses on patients' stated willingness to switch from ETI to vanzacaftor/tezacaftor/deutivacaftor (VTD), and on the factors associated with this intention, including treatment satisfaction, knowledge and expectations regarding VTD, quality of life, treatment adherence, reported adverse effects, access-related concerns and desired support from an advanced practice nurse. The quantitative component uses a study-specific questionnaire and routine-care CFQ-R 14+ and Morisky-8 data. A qualitative component consists of semi-structured interviews at the Roscoff cystic fibrosis centre.

Status (registry)
Recruiting
Study type
Observational
Enrollment
343 (estimated)
First submitted
13 Oct 2026
Start date
9 Jul 2026
Primary completion date
Dec 2026
Lead sponsor
Fondation Ildys
NCT number
NCT07885410

What you commit to

  • Study type: Observational
  • Planned participants: 343
  • From 9 Jul 2026 to the primary completion date, Dec 2026
  • 12 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

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

Prior treatment

  • Currently receiving the new CFTR modulator VTD

Other

  • Patient objects to the use of their data for this project\\n•

Who the study is looking for

  • Diagnosis of cystic fibrosis
  • Currently treated with ETI for at least 3 months, OR previously treated with ETI but treatment discontinued for medical reasons

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (12)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
CRCM Caen
Coordinator of this site? Confirm its status
CaenFranceNot yet recruiting
CRCM Giens
Coordinator of this site? Confirm its status
GiensFranceRecruiting
CRCM Grenoble
Coordinator of this site? Confirm its status
GrenobleFranceRecruiting
CRCM Lille
Coordinator of this site? Confirm its status
LilleFranceNot yet recruiting
CRCM Lyon
Coordinator of this site? Confirm its status
LyonFranceNot yet recruiting
CRCM Montpellier
Coordinator of this site? Confirm its status
MontpellierFranceRecruiting
CRCM Paris
Coordinator of this site? Confirm its status
ParisFranceNot yet recruiting
CRCM Reims
Coordinator of this site? Confirm its status
ReimsFranceRecruiting
CRCM Rennes adultes
Coordinator of this site? Confirm its status
RennesFranceNot yet recruiting
Fondation ILDYS
Coordinator of this site? Confirm its status
RoscoffFranceRecruiting
CRCM Rouen
Coordinator of this site? Confirm its status
RouenFranceRecruiting
CRCM Vannes
Coordinator of this site? Confirm its status
VannesFranceNot yet recruiting

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