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Completed

NCT Number: NCT06331000

Effect of One Year Elexacaftor-tezacaftor-ivacaftor Treatment

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.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Hopitaux Universitaires de Strasbourg

Strasbourg, 67000, France

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 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

Exclusion criteria

  • Patient not eligible for triple CFTR modulator
  • Patient intolerant to triple corrector
  • Pregnant woman

Treatment and study plan

elexacaftor-tezacaftor-ivacaftor treatment

Drug

Effect of one year elexacaftor-tezacaftor-ivacaftor treatment on glucose tolerance abnormalities in adult patients with cystic fibrosis

Primary outcomes

  1. Evaluate time in range of blood glucose variation >140 mg/dl during 2 weeks in a cohort of adult patients treated for one year with elexacaftor-tezacaftor-ivacaftor

    Time frame: time in range of blood glucose variation >140 mg/dl one year before and one year after the begining of elexacaftor-tezacaftor-ivacaftor treatment

Secondary outcomes

  1. Evaluate other CGM parameters : time in range of blood glucose >180mg/dl ; >140mg/dl ; <70mg/dl ; 70-180 mg/dl ; 70-140mg/dl

    Time frame: One year before and one year after the start of elexacaftor-tezacaftor-ivacaftor treatment

  2. Marker of metabolic status: HbA1c (mmol/l)

    Time frame: One year before and one year after the start of elexacaftor-tezacaftor-ivacaftor treatment

  3. Marker of metabolic status: HbA1c (%)

    Time frame: One year before and one year after the start of elexacaftor-tezacaftor-ivacaftor treatment

  4. Marker of metabolic status: C-Peptid (µg/L)

    Time frame: One year before and one year after the start of elexacaftor-tezacaftor-ivacaftor treatment

  5. Marker of metabolic status: C-Peptid (nmol/L)

    Time frame: One year before and one year after the start of elexacaftor-tezacaftor-ivacaftor treatment

  6. Markers of nutritional status: Evaluation of weight monitoring (kg)

    Time frame: One year before and one year after the start of elexacaftor-tezacaftor-ivacaftor treatment

  7. Markers of nutritional status: Body Mass Index (BMI)

    Time frame: One year before and one year after the start of elexacaftor-tezacaftor-ivacaftor treatment

  8. Diabetes treatment (assess insulin needs) : mean glucose value per day (mg/dl)

    Time frame: One year before and one year after the start of elexacaftor-tezacaftor-ivacaftor treatment

  9. Assessment of respiratory function parameters : number of IV antibiotics

    Time frame: One year before and one year after the start of elexacaftor-tezacaftor-ivacaftor treatment

  10. Number patients with severe hypoglycaemia and serious adverse events

    Time frame: One year before and one year after the start of elexacaftor-tezacaftor-ivacaftor treatment

Sponsors and collaborators

Lead sponsor

University Hospital, Strasbourg, France

Other

Registry information

Official study title

DIATRIM : Effect of One Year Elexacaftor-tezacaftor-ivacaftor Treatment on Glucose Tolerance Abnormalities in Adult Patients With Cystic Fibrosis.

Acronym: DIATRIM

Important dates

Study start
2024
Primary completion
2025
Study completion
2025
First posted
Mar 26, 2024
Registry last updated
May 8, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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