CClinicalTrials.gg
CompletedNCT03197909Updated Apr 18, 2019

Involvement of Plasmatic Factors in the Peripheral Muscle Dysfunction of COPD Patients - In Vitro Study

An observational study in Chronic Obstructive Pulmonary, sponsored by University Hospital, Montpellier. Completed at 1 site in France. Open to participants aged 35 Years to 85 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2019-04-18.

Sponsored by University Hospital, Montpellier · Observational

Study type
Observational
Model
Case-control
Time perspective
Retrospective
Enrollment
18
Ages
35 Years to 85 Years
Sex
All
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Study summary

Chronic Obstructive Pulmonary Patients is a defined by persistent airflow limitation that is usually progressive and associated with an enhanced chronic inflammatory response in the airways and the lung to noxious particles or gases. It is associated with an atrophy of the skeletal muscle that impairs the patient's prognosis. The biological mechanisms of this muscle atrophy have not been elucidated, and the "spill-over theory" has recently emerged. Indeed, in COPD patients, the pulmonary inflammation is associated with a systemic low-grade inflammation, and the increased pro-inflamatory molelcules in the blood - which constitute the cellular micro-environement of the muscle fibre - could activate the mechanisms of the cell atrophy.

02

Conditions studied

  • Chronic Obstructive Pulmonary

Keywords

  • COPD (Chronic Obstructive Pulmonary Patients)
  • Atrophy
  • cell cultur
  • systemic inflammation
  • Catabolism
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In context

Lead sponsor

University Hospital, Montpellier is the lead sponsor of 1,244 studies on the registry; 225 are open to participants now.

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

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Who can participate

Ages eligible
35 Years to 85 Years
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

Chronic Obstructive Pulmonary Patients

Inclusion criteria

35 to 85 years old

  • COPD patients: association of symtoms (breathlessness, cough, sputum) and chronic exposure to inhalated risk factors (like tobacco smoke) and a FEV1/VC ratio \<70% assessed by a spirometry
  • Healthy subjects: A sedentariness assessed by a Voorrips score \<9.4 and/or a report of \<150 min/week of moderate-to-vigorous physical activity

Exclusion criteria

Exclusion Criteria:

  • A recent COPD exacerbation (\< 4weeks)
  • The decompensation of a comorbidity
  • An antioxidant supplementation or medication
  • A long-term systemic corticosteroid medication
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Study design

Observational model
Case-control
Time perspective
Retrospective
Enrollment
18 participants (actual)
Patient registry
No

Groups and cohorts

  • Healthy subjects

    Determination of pro-inflammatory plasma factors at Healthy subjects aged from 35 to 85 years old

    Other: Determination of pro-inflammatory plasma factors

  • COPD patients

    Determination of pro-inflammatory plasma factors at COPD patients aged from 35 to 85 years old

    Other: Determination of pro-inflammatory plasma factors

Interventions

  • OtherDetermination of pro-inflammatory plasma factors

    Determination of pro-inflammatory plasma factors at COPD patients aged from 35 to 85 years old and Healthy subjects aged from 35 to 85 years old

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What researchers measure

Primary outcomes

  1. Myotube diameter of in vitro cultured myotubes

    Myotube diameter of in vitro cultured myotubes from healthy subjects, exposed to the serum of healthy controls and COPD patients

    Time frame: 6 days

Secondary outcomes

  1. Expression and translation of markers of

    Expression and translation of markers of anabolic and catabolic pathways

    Time frame: 6 days

Other outcomes

  1. Level of pro-Inflamatory markers

    Level of pro-Inflamatory markers in the serum

    Time frame: 6 days

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Study locations

1 site
  • Uhmontpellier
    Montpellier, 34290, France
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References and documents

Individual participant data

Plan to share: Undecided — NC

No publications or documents are linked to this record.

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Apr 18, 2019, 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
NCT03197909
Lead sponsor
University Hospital, Montpellier
Responsible party
Sponsor
First posted
Jun 23, 2017
Start date
Jul 6, 2017
Primary completion
Dec 31, 2018
Completion
Jan 31, 2019
Last update
Apr 18, 2019

Study contacts

Maurice HAYOT, MD, PhD
study director · University Hospital, Montpellier

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Sep 2018. You cannot join it, but the record below documents what was studied.

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