ENDURANCE: Analysing Peripheral Skeletal Muscle Function Before and After Endobronchial Valve Treatment

Sponsor
University Medical Center Groningen (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT06025500
Collaborator
(none)
15
21

Study Details

Study Description

Brief Summary

Rationale: Chronic obstructive pulmonary disease (COPD) is characterised by a high prevalence of peripheral muscle dysfunction, which can have significant clinical consequences, including decreased exercise capacity, reduced quality of life, and even a higher mortality rate. Reduction of lung hyperinflation using bronchoscopic lung volume reduction treatment with one-way endobronchial valves (EBV) is a minimally invasive intervention which improves exercise capacity and physical activity in patients with severe emphysema. This positive effect is also related to weight gain and alterations in body composition. The physiologic and structural adaptations of skeletal muscle function after EBV treatment has never been investigated before.

Objective: To investigate the physiological and structural adaptations of peripheral muscle function at a cellular level in response to EBV treatment.

Study design: A single center, prospective clinical trial with a single-arm pretest-posttest design. Patients with severe emphysema who will receive a bronchoscopic lung volume reduction treatment are asked to undergo additional in-magnet exercise testing and muscle biopsies before and after placement of EBVs.

Study population: Patients with severe emphysema who are scheduled to undergo EBV treatment.

Main study parameters/endpoints: The difference in quadriceps phosphocreatine concentration (PCr), quadriceps inorganic phosphorus concentration (Pi), and quadriceps pH at rest, during progressive exercise, and recovery rate will be measured by 31P-MRS to assess the physiological effect of EBV treatment on skeletal muscle function and its bioenergetics. Furthermore, we will perform a detailed histological and biochemical analysis of muscle fiber type composition, mitochondrial density, master regulators of muscle oxidative programming, and mitochondrial respiration before and after EBV treatment.

Condition or Disease Intervention/Treatment Phase
  • Diagnostic Test: 31P-Magnetic Resonance Spectroscopy (31P-MRS)

Study Design

Study Type:
Observational
Anticipated Enrollment :
15 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Analysing cEllular Bioenergetics aNd Structural aDaptations in the qUadriceps Muscle befoRe and After endobroNChial Valve treatmEnt
Anticipated Study Start Date :
Mar 1, 2024
Anticipated Primary Completion Date :
Dec 1, 2025
Anticipated Study Completion Date :
Dec 1, 2025

Arms and Interventions

Arm Intervention/Treatment
EBV-patients

Patients who are scheduled for a bronchoscopic lung volume reduction treatment using endobronchial valves.

Diagnostic Test: 31P-Magnetic Resonance Spectroscopy (31P-MRS)
31P-Magnetic Resonance Spectroscopy will be performed during exercise testing.
Other Names:
  • Muscle biopsy
  • Outcome Measures

    Primary Outcome Measures

    1. Change in quadriceps phosphocreatine concentration measured by 31P-MRS. [6 months]

      To assess the physiological adaptations, in terms of cellular bioenergetics, of the quadriceps muscle in patients with severe COPD in response to EBV treatment. This will be done by performing 31P-MRS during exercise testing in a MR-compatible ergometer at baseline and at 6 months follow-up, for which the quadriceps phosphocreatine concentration (PCr) at rest and during progressive exercise will be assessed.

    Secondary Outcome Measures

    1. Change in muscle fiber type composition measured in muscle biopsies. [6 months]

      Change in muscle fiber type composition 6 months after EBV treatment measured in muscle biopsies.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    N/A and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Patient is scheduled for a bronchoscopic lung volume treatment using one-way endobronchial valves;

    • Patient read, understood and signed the Informed Consent Form.

    Exclusion Criteria:
    • Inability to perform a cycle ergometry test;

    • Contraindications for undergoing a magnetic resonance imaging scan (e.g. claustrophobia, implanted cardiac devices);

    • Body length >190cm;

    • Any anticoagulant therapy;

    • COPD exacerbation 4 weeks prior to testing.

    Contacts and Locations

    Locations

    No locations specified.

    Sponsors and Collaborators

    • University Medical Center Groningen

    Investigators

    • Principal Investigator: Dirk-Jan Slebos, MD PhD, UMC Groningen

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Dirk-Jan Slebos, Head of the department of Pulmonary Diseases and Pulmonologist, University Medical Center Groningen
    ClinicalTrials.gov Identifier:
    NCT06025500
    Other Study ID Numbers:
    • ENDURANCE
    First Posted:
    Sep 6, 2023
    Last Update Posted:
    Sep 8, 2023
    Last Verified:
    Sep 1, 2023
    Individual Participant Data (IPD) Sharing Statement:
    Undecided
    Plan to Share IPD:
    Undecided
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Sep 8, 2023