Prevalence of Asymptomatic Thrombosis in Multiple Myeloma

Status

Withdrawn

Phases

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT03145870

Enrollment

Registered

2017-05-09

Start date

2014-06-03

Completion date

2017-05-16

Last updated

2020-07-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Multiple Myeloma, Thrombosis

Brief summary

Malignant hemopathies, such as solid cancers, increase the risk of venous and arterial thromboembolic events. The incidence of symptomatic venous thromboembolic events is particularly high in myeloma, linked to the usual risk factors for venous thromboembolic disease, biological risk factors specific to myeloma, and especially to its treatments. The prevalence of asymptomatic venous thromboembolic events and arterial events are not known to date and remain important data for planning a possible randomized study to determine the most suitable thromboprophylaxis in these patients.

Interventions

OTHEREchoing of the lower limbs and measuring the systolic pressure index

Echoing of the lower limbs and measuring the systolic pressure index

Study design

Allocation

Intervention model

SINGLE_GROUP

Primary purpose

OTHER

Masking

NONE

Eligibility

Sex/Gender

ALL

Age

18 Years to No maximum

Healthy volunteers

Inclusion criteria

* Patient major age ≥18 years * Patients with symptomatic myeloma meeting the definition of the International Myeloma Working Group, regardless of the therapeutic line, including patients in remission and untreated. * Patient having given informed consent, signed. * Patient benefiting from a social security scheme

Exclusion criteria

* Patients with non-symptomatic myeloma (stage I) or gammapathy of unknown significance (MGUS). * Patient undergoing antithrombotic treatment for deep or superficial venous thrombosis and / or pulmonary embolism at the time of inclusion. * Patients with occlusive arterial disease of the lower limbs known at the time of inclusion. * Minors, protected adults and patients deprived of liberty or not affiliated to a social security scheme * Pregnant woman * Patient unable to express consent. * Patient under guardianship or curatorship or patient deprived of public liberty

Design outcomes

Primary

Measure	Time frame
Analysis of the occurrence of venous thromboembolic events via transverse Doppler echo	1 day

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026