SARCO-COVID: Sarco-COVID Study: Measuring the Loss of Skeletal Muscle Mass in the Hospitalized Patient With the Diagnosis of COVID-19

Sponsor
Fundacion para la Investigacion Biomedica del Hospital Universitario la Paz (Other)
Overall Status
Recruiting
CT.gov ID
NCT04780126
Collaborator
(none)
64
1
3.1
20.7

Study Details

Study Description

Brief Summary

The COVID-19 pandemic is having a devastating global impact, and older adults who experience it are at higher risk of death from the disease. However, survivors of the disease have a greater risk of suffering from pathologies such as sarcopenia, which is more frequent in younger adults and with greater severity of the disease.

Sarcopenia is present in 5-13% of people between 60 and 70 years old and in 11-50% of the population over 80 years of age. The diagnosis of sarcopenia has advanced in recent years by establishing homogeneous criteria in different consensuses that necessarily combine two elements: generalized loss of strength accompanied by loss of skeletal muscle mass. Today there are three consensuses for the diagnosis of sarcopenia: the international (IWGS), the European (EWGSOP), and the most recent from a US cohort (FNIH). In all of them, the measurement of skeletal muscle mass constitutes one of the two diagnostic criteria.

The main methods to measure this muscle loss that are established are imaging techniques (computerized tomography (CT), magnetic resonance imaging (MRI), dual-energy X-ray absorptiometry (DEXA) and ultrasound.

The most common ultrasound measurements used for this purpose are the muscle thickness (cm) at the point of the ultrasound path of maximum muscle thickness, the cross-sectional area (area calculated by the basic software at the point of maximum muscle thickness), and the pennation angle (angle formed between deep muscle fascia and muscle fibers). The first two measurements can be made on several long muscles, while the pennation angle is usually made primarily on the medial gastrocnemius (internal twin) muscle. They are easy to obtain, bloodless, and reproducible measurements.

Research efforts at this point in the pandemic should focus on the longer-term consequences of the disease, sequelae such as sarcopenia in patients who have suffered from COVID-19. At the same time, clinicians must become increasingly aware of the condition and its measurement integrated into clinical practice. The knowledge provided by studies such as the one presented will allow the development of specific interventions.

The risk of sarcopenia should be considered when carrying out a risk / benefit assessment of the established treatment (for example, dexamethasone), and considering a multidisciplinary treatment that includes dietary inputs.

Condition or Disease Intervention/Treatment Phase
  • Other: Sarcopenia diagnosis

Detailed Description

Patients over 18 years of age who are admitted to the hospital and whose main diagnosis and reason for staying is COVID-19 pneumonia will be included. The prevalence of sarcopenia in hospitalized patients is 15-20%. Assuming an alpha risk of 0.05 and a beta risk of 0.2 in a unilateral contrast, 64 subjects are required to detect a difference equal to or greater than 20% loss of muscle mass. A loss to follow-up rate of 0% has been estimated.

Study Design

Study Type:
Observational [Patient Registry]
Anticipated Enrollment :
64 participants
Observational Model:
Ecologic or Community
Time Perspective:
Prospective
Official Title:
Measuring the Loss of Skeletal Muscle Mass in the Hospitalized Patient With the Diagnosis of COVID-19
Actual Study Start Date :
Feb 26, 2021
Anticipated Primary Completion Date :
Apr 30, 2021
Anticipated Study Completion Date :
May 31, 2021

Arms and Interventions

Arm Intervention/Treatment
COVID-19 pneumonia patients

Patients over 18 years of age who are admitted to the hospital and whose main diagnosis and reason for staying is COVID-19 pneumonia will be included.

Other: Sarcopenia diagnosis
History, physical, laboratory and ultrasound parameters to diagnose sarcopenia

Outcome Measures

Primary Outcome Measures

  1. Loss of muscle mass [1 month]

    Quantify the loss of muscle mass in hospitalized patients in areas of Internal Medicine with a diagnosis of COVID-19

Secondary Outcome Measures

  1. Prevalence of sarcopenia [1 month]

    Analyze the clinical characteristics and the prevalence of sarcopenia in the patients included in the study.

  2. Normal values of muscle ultrasound thickness [1 month]

    Analyze the thickness of the rectus femoris, vastus medialis, vastus lateralis, medial gastrocnemius in all patients.

  3. C reactive protein (CRP) correlated to the presence of sarcopenia [1 month]

    Analyze the correlation between CRP and the presence of sarcopenia

  4. Therapy with corticosteroids impact on muscle thickness [1 month]

    Determine the correlation between muscle thickness and the corticotherapy received (dexamethasone, methylprednisolone, prednisone)

  5. Normal values of medial gastrocnemius pennation angle in all patients [1 month]

    Measure medial gastrocnemius pennation angle in all patients

  6. Ferritin correlated to the presence of sarcopenia [1 month]

    Analyze the correlation between Ferritin and the presence of sarcopenia

  7. Fibrinogen correlated to the presence of sarcopenia [1 month]

    Analyze the correlation between Fibrinogen and the presence of sarcopenia

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Over 18 years old, men or women.

  • Main diagnosis is pneumonia due to COVID-19

  • Subjects who, after having received information about the design, the purposes of the project, the possible risks that may arise from it and who at any time may deny their collaboration, verbally grant their consent to participate in the study.

Exclusion Criteria:
  • Refusal of the patient to participate in the study.

  • Present a malignant neoplasm in active phase except spino- or basal cell Ca in local stage

  • Clinical situation of agony.

  • Amputation of limb (s).

Contacts and Locations

Locations

Site City State Country Postal Code
1 Hospital de Emergencias Isabel Zendal Madrid Spain 28046

Sponsors and Collaborators

  • Fundacion para la Investigacion Biomedica del Hospital Universitario la Paz

Investigators

  • Principal Investigator: Yale Tung Chen, MD PhD, Hospital Universitario Puerta de Hierro

Study Documents (Full-Text)

More Information

Publications

None provided.
Responsible Party:
Yale Tung Chen, Principal Investigator, Fundacion para la Investigacion Biomedica del Hospital Universitario la Paz
ClinicalTrials.gov Identifier:
NCT04780126
Other Study ID Numbers:
  • 21/090-E_COVID
First Posted:
Mar 3, 2021
Last Update Posted:
Mar 3, 2021
Last Verified:
Mar 1, 2021
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
Keywords provided by Yale Tung Chen, Principal Investigator, Fundacion para la Investigacion Biomedica del Hospital Universitario la Paz
Additional relevant MeSH terms:

Study Results

No Results Posted as of Mar 3, 2021