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Cystic FibrosisCHRONO-MUCONCT06370962

Circadian Rhythm Disorders in Children With Cystic Fibrosis Under CFTR (Cystic Fibrosis Transmembrane Conductance Regulator) Modulators

An observational study of Cystic Fibrosis, run by Hospices Civils de Lyon at 3 sites in France.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial summary

Cystic fibrosis (CF) is a rare disease affecting one out of 4,500 newborns in France (INSERM 2021). Despite major advances in patient care over the past two decades, with significant improvements in life expectancy, cystic fibrosis remains a pathology that considerably impairs quality of life. Read more about this study

Who is it for?
Ages 2 to 17 years
Conditions the study is for
Cystic Fibrosis
How many people
180 participants
Where
3 sitesFrance
Study dates
29 Apr 2024to 29 Jan 2026
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 2 to 17 years
  • All sexes
  • No healthy volunteers
  • Child

Study population: Patients will be selected from Cystic Fibrosis Resource and Skill Centres of pediatric tertiary care hospitals (Lyon, Paris-Trousseau, Nancy).

Who may be able to join

  • Patients with cystic fibrosis
  • Aged from 2 to 17 years and 11 months
  • Treated with CFTR modulator Kaftrio-Kalydeco from at least 2 months
  • Followed in Lyon, Paris-Trousseau or Nancy Cystic Fibrosis Resource and Skill Centres
  • Non-opposition from both parents

Who cannot join

  • Parental refusal
  • Parents unable to comply with protocol requirements at investigator's discretion
  • Subject participating in interventional research with an exclusion period still in progress at the time of inclusion

Trial locations and contacts

3 sites in 1 country.

France3 sites, 3 recruiting
  • Hôpital Femme Mère Enfant

    Bron, 69677

    Laurianne COUTIER, MD;PhD, 04 27 85 50 42 ext. +33, laurianne.coutie@chu-lyon.fr

    Laurianne COUTIER, MD;PhD

    Recruiting
  • Service de pédiatrie, CHRU de Nancy - Hôpitaux de Brabois

    Nancy, 54500

    Iulia IOAN, MD, 03.83.15.47.94 ext. +33, ic.ioan@chru-nancy.fr

    Iulia IOAN, MD

    Not yet recruiting
  • Service de pneumologie pédiatrique, Hôpital Armand Trousseau

    Paris, 75012

    Jessica TAYTARD, MD, 01 44 73 63 46 ext. +33, jessica.taytard@aphp.fr

    Jessica TAYTARD, MD

    Not yet recruiting

Other trials in France

About this study

Official title: Overview of Circadian Rhythm Disorders in Children With Cystic Fibrosis in the Era of CFTR (Cystic Fibrosis Transmembrane Conductance Regulator) Modulators

Cystic fibrosis (CF) is a rare disease affecting one out of 4,500 newborns in France (INSERM 2021). Despite major advances in patient care over the past two decades, with significant improvements in life expectancy, cystic fibrosis remains a pathology that considerably impairs quality of life.

Several studies have reported the possibility of respiratory and non-respiratory sleep disorders (SD) in patients with CF. Respiratory disorders are reported to affect 30% of children with CF (Barbosa 2020). Among non-respiratory SD, sleep onset and maintenance insomnia are well known in these patients, while chronotype abnormalities (circadian rhythm disorders) are understudied. Chronotype refers to a person's tendency to be more efficient in the morning or evening.

Read more

The existence of chronotype abnormalities has been suggested in CF patients, but no precise data are available (Louis 2022). The involvement of CFTR (Cystic Fibrosis Transmembrane Conductance Regulator) protein dysfunction in the central nervous system (CNS) has been hypothesized as a contributory factor. In vivo, in a mouse model of CF, dysregulation of clock genes such as Clock, Cry2 and Per2 was found in the CNS (Barbato 2019). Among them, certain genes such as Rev-erbα could regulate endobronchial inflammation and contribute to the severity of respiratory pathology. All in all, chronotype abnormalities could be at the origin of sleep debt, impaired cognitive functions or metabolic disturbances.

In the era of highly effective modulator therapy (HEMT) for the treatment of CF, the impact of these new therapies on chronotype has been understudied. Assuming that chronotype abnormalities are a direct consequence of CFTR protein dysfunction in the retina and anterior hypothalamus, HEMT should improve sleep quality. However, between 20% and 30% of adult and pediatric patients express an increase in chronotype abnormalities following initiation of treatment.

Paradoxically, the perceived gain in respiratory quality of life is counterbalanced by the occurrence of these disorders. Some patients would effectively reverse their treatment in order to limit the phenomenon. A single polysomnographic study evaluated the effect of HEMT Kaftrio-Kalydeco on sleep in adults with CF (Welsner 2022). After 3 months of treatment, patients had a significant reduction in respiratory events, with no change in total sleep time, sleep efficiency or sleep architecture. Chronotype was not mentioned. Currently, no studies on chronotype in children or adults with CF have been carried out. Our hypothesis is that CF patients treated with HEMT would develop an abnormal chronotype of late sleep onset.

The aim of this study is to evaluate the chronotype of children with CF treated with HEMT. Chronotype abnormalities could have major consequences for quality of life, the immune system, cognitive functions and metabolism. Systematic detection of these disorders via anamnesis, followed by diagnosis by questionnaire, actimetrics and/or urinary melatonin dosage, would enable their early management, starting with the reversal of Kaftrio-Kalydeco intake between morning and evening.

Conditions
Cystic Fibrosis
Keywords
cystic fibrosis, Cystic fibrosis transmembrane conductance regulator modulators, circadian rhythm disorders
Medical subject headings
Cystic Fibrosis, Chronobiology Disorders

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

Study groups in NCT06370962
Study groupRoleWhat they receive
Children and adolescents with cystic fibrosis treated with Kaftrio-KalydecoPatients with cystic fibrosis Aged from 2 to 17 years and 11 months Treated with CFTR modulator Kaftrio-Kalydeco for at least 2 months Followed in a participating Cystic Fibrosis Resource and Skill national Centre

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Result of the Horne and Ostberg questionnaire.

    The frequency of each chronotype (normal, morning or evening) in patients with CF on HEMT will be determined by the result of the Horne and Ostberg questionnaire.

    The frequency of each chronotype will be summarized for all CF patients on HEMT using the following descriptive statistics: frequencies and percentages for each level of the variable (normal, morning or evening) and the number of missing values (missing values will be counted but not included in the denominator of the frequency calculation).

    Scores from 5 to 25: 21-25 = clearly morning; 18-20 = moderately morning; 12-17 = nor morning, neither evening; 9-11: moderately evening; 5-8: clearly evening.

    Measured: Day 0

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted17 Apr 2024
  2. Study start29 Apr 2024
  3. Primary completion29 Oct 2025 (estimated)
  4. Study completion29 Jan 2026 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
180 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06370962
Sponsor's protocol ID
69HCL24_0076
Other IDs
2024-A00343-44
Acronym
CHRONO-MUCO
Status last verified
Sep 2024
First submitted
19 Feb 2024
Last updated
20 Sep 2024
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

An observational study of Cystic Fibrosis, run by Hospices Civils de Lyon at 3 sites in France.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 5 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: status not confirmed, as of the sponsor's last update on 20 Sep 2024. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 3 sites in France. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

Contact Laurianne COUTIER, MD (04 27 85 50 42 ext. +33, laurianne.coutie@chu-lyon.fr), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Result of the Horne and Ostberg questionnaire. (time frame: Day 0). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 20 Sep 2024.

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