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CompletedNCT02809560CAVASTHMEUpdated Sep 21, 2026

Detection of Cav1 Calcium Channels in Inflammatory Cells of Asthmatic Children

An interventional study of Induced sputum method using hypertonic serum in Asthma, sponsored by University Hospital, Toulouse. Completed at 1 site in France. Open to participants aged 6 Years to 18 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-09-21.

Sponsored by University Hospital, Toulouse · Not applicable, Interventional, and Basic science

Phase
Not applicable
Study type
Interventional
Enrollment
60
Allocation
Non-randomized
Ages
6 Years to 18 Years
Sex
All
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Study summary

Asthma affects about 10% of children and 6% of adults in industrialized countries. Lymphocytes (L) Th2, a T cell population (LT) producing interleukin (IL) -4, 5 and 13 are broadly involved in this pathology in experimental models and in humans. Many studies show that the signaling pathways activated by the commitment of T receiver differ depending LT. The identification of specific signaling pathways links to Th2 offer new therapeutic approaches. Precedent study showed that mouse Th2 selectively expressed related to calcium channels sensitive channels Cav1 voltage, normally found in excitable cells where they are defined as receivers dihydropyridine (DHP).

The goal of the present study is to show the presence of Cav1 channels in inflammatory cells in allergic asthmatics and show overexpression of these channels in the peripheral blood mononuclear cells from asthmatic subjects before and / or after stimulation with the TCR in comparison with controls.

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Conditions studied

  • Asthma

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Keywords

  • Lymphocytes Th2
  • Cav1 channels
03

In context

Asthma

3,921 studies on the registry are indexed under Asthma; 507 are open to participants now.

This study's enrollment of 60 is below the median of 83 across 2,752 interventional studies indexed under Asthma.

Browse Asthma studies →

Lead sponsor

University Hospital, Toulouse is the lead sponsor of 794 studies on the registry; 214 are open to participants now.

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

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Who can participate

Ages eligible
6 Years to 18 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

For Asthmatic children arm :

  • Girl not in childbearing potential or taking contraceptive treatment
  • Asthma diagnosis in at least 6 months as defined by clinical symptoms (expiratory dyspnea, wheezing, sibilance) and respiratory function (reversibility of VEMS at least 12% after salbutamol administration)
  • Allergologic tests positives to airborne allergens : positive prick test and/or specific IgE > 0,35 kU/L for at least one allergen
  • Asthma severity between mild to moderate based on Global initiative for asthma classification during more than one month with inhaled corticotherapies +/- long term action beta -mimetic long compounds (salmeterol, formoterol)
  • Patient insured with a social security scheme

For control children arm :

  • Girl not in childbearing potential or taking contraceptive treatment
  • No medical history of asthma
  • No medical history of allergy or symptoms of allergy on skin (atopic dermatitis), respiratory tract (rhino-conjunctivitis, asthma) or food allergy

Exclusion criteria

Exclusion Criteria:

For both arms:

  • Chronic respiratory pathology : known occlusive or restrictive respiratory syndrome like interstitial lung disease, neuromuscular disease, mucoviscidoses, respiratory tract abnormalities with cough, dyspnea or digital hippocratism.
  • History of pulmonary or nose and throat infectious disease during last 4 months
  • Parasitic disease non treated during last 3 months
  • Dyspnea during the inclusion
  • Systemic corticotherapy during the last 3 months before inclusion
  • Immunosuppressive therapy during the last 3 months before inclusion
  • Diabeta
  • Disease causing immune disorder
  • Infection during inclusion
  • Participation to another study witch implies medical treatment during last 3 months before inclusion

For asthmatic children arm :

  • Chronic pulmonary pathology (excluding asthma)
  • Asthma exacerbation during inclusion
  • VEMS \< 70% of normal range or VEMS \< 70% of normal range after inhalation of serum (despite salbutamol administration)
  • Patient unable to complete pulmonary function testing
05

Study design

Phase
Not applicable
Primary purpose
Basic science
Allocation
Non-randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
60 participants (actual)

Study arms

  • Experimental
    Asthmatic children

    Induced sputum method using hypertonic serum

    Procedure: Induced sputum method using hypertonic serum

  • Sham comparator
    Control children

    Induced sputum method using hypertonic serum

    Procedure: Induced sputum method using hypertonic serum

Interventions

  • ProcedureInduced sputum method using hypertonic serum

    Collection of expectoration in sterile vial, conserved in ice all along the examination

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What researchers measure

Primary outcomes

  1. Detection of sequence coding for Cav1 in cells as assessed by reverse transcription polymerase chain reaction

    Time frame: Day 1

Secondary outcomes

  1. Presence of Cav1 channels as assessed by correlation between Cav1 expression and eosinophils in expectoration collection

    Time frame: Day 1

  2. Presence of Cav1 channels as assessed by correlation between Cav1 expression and lymphocytes T in expectoration collection

    Time frame: Day 1

  3. Comparison of CRTH2+ cells in total blood between asthmatic and control group

    Time frame: Day 1

  4. Comparison of Cav1 channels and cytokines Th2 expression between asthmatic and control group before T-Cell receptor stimulation

    Time frame: Day 1

  5. Comparison of Cav1 channels and cytokines Th2 expression between asthmatic and control group after T-Cell receptor stimulation

    Time frame: Day 1

07

Study locations

1 site
  • Centre Hospitalier Universitaire
    Toulouse, France
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References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 21, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT02809560
Lead sponsor
University Hospital, Toulouse
Responsible party
Sponsor
First posted
Jun 22, 2016
Start date
Mar 2013
Primary completion
May 2016
Completion
May 2016
Last update
Sep 21, 2026

Study contacts

François Brémont, MD
principal investigator · Hôpital des Enfants CHU Toulouse

Oversight

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

Not currently enrolling

This study is completed, as verified in Sep 2026. You cannot join it, but the record below documents what was studied.

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