Phase
Condition
Lymphedema
Treatment
Compressive bandaging
MOBIDERM Autofit Armsleeve
Clinical Study ID
Ages > 18 Female
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Unilateral secondary upper limb lymphedema of stage II or III according to thecriteria defined by the International Society of Lymphology, following breast cancer
Volume difference between affected and healthy arm ≥ 10%
Affected arm that fits with one of the 6 standard sizes of the Auto- AdjustableMOBIDERM Autofit armsleeve provided.
Signed informed consent prior to any study-mandated procedure.
Exclusion
Exclusion Criteria:
Stage I lymphedema or located in several places.
Patients for whom compression is contraindicated.
Lymphedema associated with active cancer needing acute chemotherapy or havingrecurrence or metastasis.
Motor and sensitive neurological deficiency / psychiatric or addictive disorders
Pregnant or breastfeeding patient
Patient intolerant to MOBIDERM Autofit or known allergies to the components used.
Participation to any other clinical study which has an impact on the differentendpoints
Vulnerable patient, adults being the object of a legal protective measure or enableto express their consent.
Study Design
Study Description
Connect with a study center
ANKARA
Ankara,
TurkeyActive - Recruiting
Pinar BORMAN
Ankara,
TurkeyActive - Recruiting
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