Lymphedema Clinical Trial
Official title:
Comfort Subcutaneous Drainage: a Descriptive Study Among Palliative Care Cancer Patients Presenting Severe Refractory Lower Limbs Lymphedema
Verified date | November 2023 |
Source | Centre Hospitalier Universitaire de Nice |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Physical embarrassment, pain and psychological impact linked to the body image distortion are often associated to these lymphedemas. Investigators decided to study new therapeutic method because of major discomfort due to these oedemas and doctors' difficulty to manage them. Subcutaneous drainage also called lymphocentesis seems to be an interesting technique. This local treatment consists in inserting in lower limbs several catheters draining into enclosed bags in order to evacuate lymph fluid and to lower local pressure. Very few studies have been published concerning this technique and are presenting only a small number of cases. They cannot allow clear conclusions of this technique's efficiency but show encouraging results. Investigators want to collect more data on this technique using a larger number of subjects in order to evaluate subcutaneous drainage effects on the comfort of palliative care cancer patients presenting lower limbs lymphedema. Investigators will consider as lymphedema, oedemas with no renal or cardiovascular identified cause and excluding anasarca.
Status | Completed |
Enrollment | 24 |
Est. completion date | September 15, 2018 |
Est. primary completion date | September 15, 2018 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - Cancer patients - Palliative care patients according to the SFAP (French Palliative care society) definition - Patient taken care of in one of the palliative care structures implied in this project (palliative care unit, palliative care field team, hospital at home, palliative care day hospital) - Patients presenting lower limb lymphedema resistant to traditional treatments or for whom these treatments are not adapted - Lymphedema being a source of discomfort for the patient asking for relief - Patient wishing a new treatment for lymphedema - Patients with full cognitive capacities evaluated by the practitioner in charge of him - Patients available during the study Exclusion Criteria: - Lost-of-sight or transferred to another hospital subjects - Subjects wishing to end their participation before study ending |
Country | Name | City | State |
---|---|---|---|
France | Centre Hospitalier | Avignon | |
France | CAL | Nice | Alpes-maritimes |
France | Centre Hospitalier Universitaire de Nice | Nice |
Lead Sponsor | Collaborator |
---|---|
Centre Hospitalier Universitaire de Nice |
France,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | evolution of the patient's discomfort due to his oedemas | It will be measured with a numeric scale from 0 no discomfort to 10 maximal discomfort. | on the 3rd day after lymphcentesis |
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