Lymphedema Clinical Trial
— LymphFMOfficial title:
Typing of Gut Microbiota in Patients With Limb Lymphedema and Recurrent Lymphangitis, a Prospective Observational Study
NCT number | NCT06228937 |
Other study ID # | 6208 |
Secondary ID | |
Status | Recruiting |
Phase | |
First received | |
Last updated | |
Start date | February 22, 2024 |
Est. completion date | October 30, 2028 |
Verified date | January 2024 |
Source | Fondazione Policlinico Universitario Agostino Gemelli IRCCS |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
Lymphedema is a chronic and progressive disease of the lymphatic vessels which affects about 300 million people worldwide. Patients may experience recurrent soft tissue infection of the limb affected by lymphedema, in terms of erysipelas, lymphangitis or cellulitis. No previous study has ever investigated the possible role of the gut microbiota in the genesis of acute infectious/inflammatory episodes in these patients. Our hypothesis is that lymphedema patients with recurrent soft tissue infections are characterized by pro-inflammatory changes in the microbiota.
Status | Recruiting |
Enrollment | 60 |
Est. completion date | October 30, 2028 |
Est. primary completion date | October 30, 2027 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 85 Years |
Eligibility | Inclusion Criteria (Group A): - 18-85 years - primary or secondary, upper or lower limb lymphedema, I-II-III stage ISL - at least 3 episodes of soft tissue infection in an year, in the last 2 years - consent to participate in the study Inclusion Criteria (Group B): - 18-85 years - primary or secondary, upper or lower limb lymphedema, stage I-II-III (ISL) - no episodes of soft tissue infection in the last 2 years - consent to participate in the study Exclusion Criteria: - No compliance to perform limb compression and skin hygiene - Antibiotic therapy in the last 15 days - Diabetes mellitus - Immunodeficiency - Ongoing neoplastic pathology - Taking immunosuppressive drugs - Unavailability to follow-up for at least 24 months post-enrollment. |
Country | Name | City | State |
---|---|---|---|
Italy | Fondazione Policlinico Universitario Agostino Gemelli IRCCS | Rome |
Lead Sponsor | Collaborator |
---|---|
Fondazione Policlinico Universitario Agostino Gemelli IRCCS |
Italy,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | comparison alpha diversity | comparison alpha diversity of the gut microbiota in groups A and B | 60 months | |
Secondary | comparison beta diversity | comparison beta diversity of the gut microbiota in groups A and B | 60 months | |
Secondary | evaluation of the microbiome differential abundance | evaluation of the microbiome differential abundance to identify taxa associated | 60 months |
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