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Muscle Dysfunction in Patients With Haematological Diseases

Rigshospitalet logo

Rigshospitalet

Status

Active, not recruiting

Conditions

Acute Lymphoid Leukemia
Lymphoma
Myelodysplastic Syndromes
Acute Myeloid Leukemia
Hematologic Diseases

Study type

Observational

Funder types

Other

Identifiers

NCT05150561
MuscleLab2020

Details and patient eligibility

About

PURPOSE: To evaluate the prevalence and prognostic value of sarcopenia in patients diagnosed with hematological cancer diseases.

Full description

Some patients diagnosed with malignant hematological diseases are faced with poor prognosis and thus must undergo a demanding course of treatment associated with severe deconditioning potentially leading to worse prognostic outcomes. It is currently not well-described, to what extend patients body composition at the point of diagnoses should be part of standard clinical evaluation in order to optimize therapy-efficacy. Recent findings suggest that pathophysiological alterations in skeletal muscle mass and function can have significant implications for the risk of disease progression and long-term prognosis.

Enrollment

216 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

• Patients diagnosed with malignant lymphomas, acute leukaemia and multiple myeloma referred to treatment at the Department of Haematology, Rigshospitalet.

Exclusion criteria

  • Age: <18
  • Pregnancy
  • Physical or mental disabilities precluding test of muscle function
  • Inability to read and understand Danish.

Trial design

216 participants in 3 patient groups

Cohort I - Patients newly diagnosed with malignant lymphoma (n=72)
Description:
These patients will undergo two assessments: A baseline-assessment prior to treatment for the hematologic cancer disease and a follow-up assessment at 6 months after treatment start
Cohort II - Patients newly diagnosed with acute leukaemia (n=72)
Description:
These patients will undergo two assessments: A baseline-assessment prior to treatment for the hematologic cancer disease and a follow-up assessment at 6 months after treatment start
Cohort III - Patients newly diagnosed with multiple myeloma (n=72)
Description:
These patients will undergo two assessments: A baseline-assessment prior to treatment for the hematologic cancer disease and a follow-up assessment at 6 months after treatment start

Trial contacts and locations

1

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Central trial contact

Charlotte Noerregaard Groenset, MSc; Jan Christensen, PhD

Data sourced from clinicaltrials.gov

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