NCT06331000Completed
Effect of One Year Elexacaftor-tezacaftor-ivacaftor Treatment
DIATRIM : Effect of One Year Elexacaftor-tezacaftor-ivacaftor Treatment on Glucose Tolerance Abnormalities in Adult Patients With Cystic Fibrosis.
Source: ClinicalTrials.gov · Last updated 8 May 2025
Brief summary (registry, in English)
The development of CFTR (cystic fibrosis conductance transmembrane regulator) modulators for people with cystic fibrosis (pwCF) and eligible for these treatments is a true therapeutic revolution. The major beneficial effect of CFTR modulators (CFTRm) on pulmonary function and the reduction of pulmonary exacerbations should have a considerable impact on the quality of life and patient's life expectancy. Data on the impact of CFTRm on glucose tolerance abnormalities are still very fragmentary. The investigators can think that their use, earlier and earlier in the history of the disease, will transform the evolutionary trajectories of patients on the respiratory, nutritional and metabolic levels. Diabetes represents a major challenge in the management of pwCF because it is a factor in morbidity and mortality at all stages of the disease, from children to patients with terminal respiratory failure requiring lung transplantation. Early abnormalities in glucose tolerance observed in childhood, before the stage of diabetes, are also associated with poor pulmonary and nutritional outcomes. Experimental data suggest a positive effect of CFTRm on insulin secretion. However, investigators do not currently know the impact of CFTRm in patients with very early glucose disorders or at the stage of diabetes treated with insulin. Recently continuous glucose measurement (CGM) devices represent very effective tools for assessing abnormalities in glucose tolerance before the stage of diabetes and for monitoring patients treated with insulin.
- Status (registry)
- Completed
- Study type
- Observational
- Enrollment
- 184 (actual)
- First submitted
- 23 Feb 2024
- Start date
- 8 Apr 2024
- Primary completion date
- 20 Feb 2025
- Lead sponsor
- University Hospital, Strasbourg, France
- Diseases
- Cystic fibrosis
- NCT number
- NCT06331000
What you commit to
- Study type: Observational
- Participants enrolled: 184
- From 8 Apr 2024 to the primary completion date, 20 Feb 2025
- 1 site 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.
Other
- Patient not eligible for triple CFTR modulator
- Patient intolerant to triple corrector
- Pregnant woman
Who the study is looking for
- Patients with cystic fibrosis aged over 18
- Patients treated for 1 year by elexacaftortezacaftor-ivacaftor
- Normal tolerant or intolerant to glucose or presenting with cystic fibrosis related diabetes treated or not with insulin
- Patient who had a continuous glucose monitoring in the 6 months before and 6 months after one year of treatment with elexacaftor-tezacaftor-ivacaftor
Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Hopitaux Universitaires de Strasbourg Coordinator of this site? Confirm its status | Strasbourg | France | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.