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NCT07851493Recruiting

Exercise Phenotyping Prior to Chemotherapy in Newly Diagnosed Multiple Myeloma (MM-Exercise)

Exercise Phenotyping Prior to Chemotherapy Initiation in Patients With Newly Diagnosed Multiple Myeloma Without Resting Echocardiographic Signs of Cardiac Involvement

Source: ClinicalTrials.gov · Last updated 5 Oct 2026

Brief summary (registry, in English)

MM-Exercise is a prospective, single-centre, observational pilot study of patients with newly diagnosed multiple myeloma who have not yet started chemotherapy and whose resting echocardiogram is unremarkable or only mildly abnormal (preserved left ventricular ejection fraction \[LVEF\] ≥50%, at most grade I diastolic dysfunction). The study tests whether a relevant proportion of these patients already exhibit a central (cardiac) limitation of exercise capacity - defined as a cardiac output to oxygen uptake slope (CO/VO2 slope) below 5 - despite the absence of overt cardiac disease on resting assessment, and whether this exercise-derived marker correlates with subclinical myocardial tissue abnormalities on cardiac magnetic resonance imaging (CMR) and with heart-failure hospitalisation and mortality over 12 months. Eighty patients referred in comparable numbers from the haemato-oncology departments will undergo a single comprehensive baseline assessment (medical and sports history, cardiac biomarkers, resting echocardiography, 6-minute walk distance, combined cardiopulmonary exercise testing with stress echocardiography \[CPETecho\], and CMR with T1-/T2-mapping and late gadolinium enhancement) prior to chemotherapy initiation, followed by in-person clinical follow-up visits 3 and 12 months after each patient's own baseline visit.

Status (registry)
Recruiting
Study type
Observational
Enrollment
80 (estimated)
First submitted
17 Sept 2026
Start date
1 Sept 2026
Primary completion date
Jan 2028
Lead sponsor
Technical University of Munich
NCT number
NCT07851493

What you commit to

  • Study type: Observational
  • Planned participants: 80
  • From 1 Sept 2026 to the primary completion date, Jan 2028
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study design.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • New York Heart Failure Association Class IV heart failure, or recent decompensated heart failure requiring inpatient recompensation
  • Suspected new or progressive coronary artery disease

Lab values

  • Severe anaemia, defined as haemoglobin \<8 g/dL at baseline

Other

  • Estimated glomerular filtration rate \<30 mL/min/1.73m², or contraindication to gadolinium-based contrast agents
  • Pregnancy or breastfeeding

Who the study is looking for

  • Histologically or cytologically confirmed newly diagnosed multiple myeloma and chemotherapy not yet initiated
  • Resting echocardiogram with preserved left ventricular ejection fraction (≥50%) and at most mild (grade I) diastolic dysfunction with no echocardiographic signs of clinically manifest cardiac involvement
  • Age 18-99 years
  • Written informed consent
  • Sufficient German or English language skills

Age in the registry: 18 years to 99 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
Department of Preventive Sports Medicine and Sports Cardiology, TUM School of Medicine and Health, Klinikum rechts der Isar
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MunichGermanyRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.