- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02794142
Oxidative Stress on Muscle Dysfunction in Hemodialysis Patient (POPEYE)
Impact of the Oxidative Stress on the Skeletal Muscle Dysfunction in Hemodialysis Patient
In hemodialysis patient (HD) a reduction of the skeletal muscle mass and strength has previously been reported. This muscle impairment constitutes an independent prognosis factor in HD patients. Oxidative stress and inflammation have been linked to the muscle impairment. The mitochondria is a classical producer and target of reactive oxygen species (ROS), and may thus constitute a central actor of the skeletal muscle impairment in HD patients. Therefore, the aim of the present study is to investigate the role of the muscle mitochondrial density on the muscle impairment in HD patients, in comparing the muscle mitochondrial density and oxidative stress in HD patients vs. healthy matched controls.
In order to assess the effect of the oxidative stress and inflammation on the muscle impairment in HD patients, muscle function assessements will be performed after renal transplantation (which lowers the oxidative stress and inflammation levels) in the HD patient group.
No therapeutic intervention will be tested in the present study.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Montpellier, France, 34295
- Montpellier University Hospital
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Age between 40-80 years old
- less than 150min by week of moderate to vigorous physical activity
- Chronic renal failure (glomerular filtration rate less than 15mL by min) requiring hemodialysis
- Patient placed on the kidney transplant waiting list of MontpellierCHU
- No indication against temporary kidney transplant
- Review cardiovascular older than two years
- Patient not under guardianship or trusteeship
- Clinically stable state Absence or recent infection within 3 months prior to inclusion Absence of progressive neoplasia No recent acute decompensation of chronic disease (thrust of heart failure, respiratory decompensated cirrhosis).
Absence of recent stroke
- musculoskeletal and neurological states of the lower limbs which allow the realization of the proposed functional tests.
- Patient has given written informed consent
- Absence of congenital or genetic degenerative muscle disease
Exclusion Criteria:
- Terminal chronic renal failure without replacement therapy
- Local anesthesic hypersensibility
- Corticosteroid treatment upper than 3 month
- COPD
- Oral anticoagulants
- Previous renal transplantation
- Subject not affiliated with a social security scheme, beneficiary or not such a plan
- Major subject protected by law or unable to consent under Article L 1121-8 of the Public Health Code
- Vulnerable person under Article L.1121-6 of the Public Health Code
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Basic Science
- Allocation: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Other: Healthy volunteers
|
|
Experimental: HD patient
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Muscle mitochondrial density assessed on a quadriceps biopsy by immunochemistry
Time Frame: 2 years
|
2 years
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Maximum voluntary contraction of the quadriceps (in Newton.meter)
Time Frame: 2 years
|
2 years
|
Collaborators and Investigators
Sponsor
Publications and helpful links
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 9459-2
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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