ClinicalTrials.gg
TerminatedNCT01586728MUCOXYUpdated Jun 15, 2015

Oxygen Therapy in Cystic Fibrosis

An interventional study of Air - oxygen and Oxygen - Air in Cystic Fibrosis, sponsored by Assistance Publique - Hôpitaux de Paris. Terminated at 1 site in France. Open to participants aged 6 Years and older. Per ClinicalTrials.gov, last updated 2015-06-15.

Sponsored by Assistance Publique - Hôpitaux de Paris · Not applicable, Interventional, and Treatment

Why this study was terminated
lack of inclusion in the study
Phase
Not applicable
Study type
Interventional
Enrollment
8
Allocation
Randomized
Ages
6 Years and older
Sex
All
01

Study summary

This is an open, multicenter, prospective, randomised and cross over study, comparing in patients with cystic fibrosis aged > 6 years, 2 periods of 6 weeks of oxygen therapy or room air, separated by a wash out period of 2 to 6 weeks.

Read the detailed description

Rationale Oxygen therapy may be proposed to patients with cystic fibrosis (CF) with nocturnal hypoxemia but the indication and benefits of oxygen therapy have not been validated in CF.

Aim of the study and main objective The aim of the study is to evaluate the improvement in nocturnal hypoxemia by the measurement of nocturnal pulse oximetry (SpO2) after 6 weeks of nocturnal oxygen therapy in stable patients with CF.

An improvement is defined by a nocturnal SpO2 > 90% during the whole night.

Objectives and secondary aims

  • Comparison of subjective sleep quality during oxygen therapy and room air after a period of 6 weeks by means of 4 validated sleep questionnaires
  • Comparison of quality of life during oxygen therapy and room air after a period of 6 weeks by means of a validated questionnaire for CF patients (CFQ).
  • Detection of the appearance or increase in nocturnal hypercapnia during oxygen therapy and room air after a period of 6 weeks
  • Comparison of a possible arterial pulmonary hypertension during oxygen therapy and room air after a period of 6 weeks by means of an echocardiography

Study design This is an open, multicentre, prospective, randomised and cross over study, comparing in individual patient two periods of 6 weeks: one period with nocturnal oxygen therapy and one period in room air, separated by a wash out period of 2 to 6 weeks.

Inclusion criteria

  • Children ≥ 6 years and adults ≥ 18 years with CF in a stable state
  • With a forced expiratory volume in one second (FEV1) ≤ 50% of predicted value
  • Having a pulse oximetry (SpO2) in room air ≤ 90% for ≥ 10% of the night and/or a SpO2 ≤ 90% for ≥ 10 minutes during the night
  • Any patient with prior noninvasive positive pressure ventilation (NPPV) but who has stopped NPPV at least 15 days before the start of the study.
  • Written approval by the patient and by the parents in case of a pediatric patient
  • Patient having the French social security coverage Non-inclusion criteria
  • Patients with a respiratory exacerbation during the last 15 days
  • Patients with NPPV or long term oxygen therapy prior to the start of the study and unable to stop this treatment
  • Impossibility of a medical examination
  • Pregnant patient or breastfeeding patient

Study protocol The study is proposed to the patients during the V0 visit, corresponding to the screening monitoring showing a nocturnal SpO2 in room air ≤ 90% for ≥ 10% of the night and/or a SpO2 ≤ 90% for ≥ 10 minutes during the night. After a period of 2 to 30 days, the written approval is obtained during a routine visit.

Thereafter, the patient will be randomised to receive either:

  1. nocturnal oxygen therapy with a stable flow to obtain a nocturnal SpO2 >90% (Oxygen period) while continuing his routine long term treatment
  2. his routine long term treatment without nocturnal oxygen therapy (Air period) During the Oxygen period, the oxygen flow will be at least 1.5 L/min. This flow may be increased up to 2L/min in case of the presence of nocturnal periods with a SpO2 ≤ 90%.

The two periods Oxygen and Air will be separated by a wash out period of 2 to 6 weeks to rule out any long lasting effect of nocturnal oxygen therapy.

At the end of the 2 periods of 6 weeks oxygen or air, the following investigations will be performed:

  • A nocturnal evaluation of gas exchange by the Sentec™ monitor (which measures SpO2 and transcutaneous carbon dioxide (PCO2)) and objective sleep quality by means of actigraphy
  • an evaluation of subjective sleep quality by means of 4 validates sleep questionnaires
  • an evaluation of quality of life by a validated CF questionnaire (CFQ)
  • spirometry with blood gases in room air
  • an echocardiography

Number of subjects Only 3 studies have evaluated the benefit of oxygen therapy on nocturnal gas exchange during one night and only one study has evaluated the benefit of oxygen therapy after a period of 26 months. This last study is limited by the small number of patients and the low compliance with oxygen therapy.

No study has evaluated the effect of oxygen therapy during a 6 weeks period. This limits the calculation of the number of subjects.

As the study is a cross over study, a number of 30 analysable patients is estimated to be sufficient for the evaluation of the primary outcome measure and the secondary outcomes. Because of the possibility of premature withdrawal, it is planned to include 50 patients.

Total duration of the study: maximum 22.5 months

Inclusion period: 18 months

Duration of participation for one patient: maximum 4.5 months

Statistical analysis and final report: 3 months

Number of participating centres: 8

Estimation of the mean number of patients included per centre: 3 patients / 3 months / centre

Expected results The results of the present study should help to define the criteria to start long term oxygen therapy and to assess the potential benefits of this treatment in stable patients with CF.

02

Conditions studied

  • Cystic Fibrosis

Browse trials for

Keywords

  • Cystic fibrosis
  • oxygen therapy
  • sleep
03

In context

Cystic Fibrosis

1,605 studies on the registry are indexed under Cystic Fibrosis; 196 are open to participants now.

This study's enrollment of 8 is below the median of 36 across 1,051 interventional studies indexed under Cystic Fibrosis.

Browse Cystic Fibrosis studies →

Lead sponsor

Assistance Publique - Hôpitaux de Paris is the lead sponsor of 3,576 studies on the registry; 1,028 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
6 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Children ≥ 6 years and adults ≥ 18 years with CF in a stable state
  • With a forced expiratory volume in one second (FEV1) ≤ 50% of predicted value
  • Having a pulse oximetry (SpO2) in room air ≤ 90% for ≥ 10% of the night and/or a SpO2 ≤ 90% for ≥ 10 minutes during the night
  • Any patient with prior noninvasive positive pressure ventilation (NPPV) but who has stopped NPPV at least 15 days before the start of the study.
  • Written approval by the patient and by the parents in case of a pediatric patient
  • Patient having the French social security coverage

Exclusion criteria

Exclusion Criteria:

  • Patients with a respiratory exacerbation during the last 15 days
  • Patients with NPPV or long term oxygen therapy prior to the start of the study and unable to stop this treatment
  • Impossibility of a medical examination
  • Pregnant patient or breastfeeding patient
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Crossover assignment
Masking
None (open label)
Enrollment
8 participants (actual)

Study arms

  • Other
    Air - oxygen

    One period in room air and one period with nocturnal oxygen therapy, separated by a wash out period of 2 to 6 weeks.

    Other: Air - oxygen

  • Other
    Oxygen - Air

    One period with nocturnal oxygen therapy and one period in room air, separated by a wash out period of 2 to 6 weeks.

    Other: Oxygen - Air

Interventions

  • OtherAir - oxygen

    1. his routine long term treatment without nocturnal oxygen therapy during 6 weeks (air period) 2. nocturnal oxygen therapy with a stable flow to obtain a nocturnal SpO2 \> 90% (oxygen period) while continuing his routine long term treatment during 6 weeks. During the oxygen period, the oxygen flow will be at least 1.5l/min. This flow may be increased up to 2L/min in case of the presence of nocturnal periods with SpO2 \<= 90%.

  • OtherOxygen - Air

    1. nocturnal oxygen therapy with a stable flow to obtain a nocturnal SpO2 \> 90% (oxygen period) while continuing his routine long term treatment during 6 weeks. 2. his routine long term treatment without nocturnal oxygen therapy during 6 weeks (air period) During the oxygen period, the oxygen flow will be at least 1.5l/min. This flow may be increased up to 2L/min in case of the presence of nocturnal periods with SpO2 \<= 90%.

06

What researchers measure

Primary outcomes

  1. the improvement in nocturnal hypoxemia by the measurement of nocturnal pulse oximetry (SpO2) after 6 weeks of nocturnal oxygen therapy in stable patients with CF

    Time frame: after a 6 weeks period

Secondary outcomes

  1. Comparison of subjective sleep quality during oxygen therapy and room air after a period of 6 weeks by means of 4 validated sleep questionnaires

    Time frame: after a 6 weeks period

  2. Comparison of quality of life during oxygen therapy and room air after a period of 6 weeks by means of a validated questionnaire for CF patients (CFQ).

    Time frame: after a 6 weeks period

  3. Detection of the appearance or increase in nocturnal hypercapnia during oxygen therapy and room air after a period of 6 weeks

    Time frame: after a 6 weeks period

  4. Comparison of a possible arterial pulmonary hypertension during oxygen therapy and room air after a period of 6 weeks by means of an echocardiography

    Time frame: after a 6 weeks period

07

Study locations

1 site
  • Service de pneumologie pédiatrique, Hôpital Armand Trousseau
    Paris, 75012, France
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 15, 2015, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT01586728
Collaborators
Vaincre la Mucoviscidose
Responsible party
Sponsor
First posted
Apr 27, 2012
Start date
Oct 2012
Primary completion
Aug 2014
Completion
Aug 2014
Last update
Jun 15, 2015

Study contacts

Brigitte FAUROUX, MD, PhD
principal investigator · Assistance Publique - Hôpitaux de Paris

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is terminated, as verified in Jun 2015. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion