Actively Recruiting
Human Amniotic Mesenchymal Cell Secretome for Neurodegeneration and Neuroinflammation
Led by Fondazione Policlinico Universitario Agostino Gemelli IRCCS · Updated on 2025-08-14
60
Participants Needed
2
Research Sites
88 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Neurodegenerative diseases are debilitating conditions characterized by chronic inflammation, leading to dysfunction of both the non-neuronal cellular components of the central nervous system and peripheral blood immune cells. Thus, it is crucial to develop an innovative therapeutic strategy that not only effectively contrast neurodegeneration but also aims to reduce inflammation. The overall aim of the study is to provide a preclinical in vitro demonstration of the immunomodulatory and pro-regenerative potential of the human amniotic mesenchymal stromal cell (hAMSC) secretome in counteracting neurodegeneration. This potential will be evaluated in three-dimensional in vitro models of neurodegenerative diseases, such as amyotrophic lateral sclerosis (ALS) and chronic demyelinating disease (multiple sclerosis - MS). To this end, the study includes sample collection from patients without pharmacological treatment and without medical devices. Patients diagnosed with ALS, patients diagnosed with MS, and healthy volunteers will be recruited to collect blood samples and skin biopsies. Patient-specific and control organoid platforms, mimicking cellular heterogeneity and tridimensional interactions within the central nervous system including the inflammatory compartment, will be developed to be used as a valuable tool to investigate the in vitro efficacy of the hAMSC secretome.
CONDITIONS
Official Title
Human Amniotic Mesenchymal Cell Secretome for Neurodegeneration and Neuroinflammation
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients with amyotrophic lateral sclerosis (ALS) aged between 50 and 60 years with similar age of onset and disease duration
- Patients recently diagnosed with multiple sclerosis (MS), aged between 20 and 50 years, considering the male-to-female ratio of approximately 2:1
- Healthy volunteers who are spouses of patients, unaffected by neurological diseases, matching age and gender ratios of patients
You will not qualify if you...
- Patients who do not consent to participate in the study
- MS patients who have received immunomodulators or corticosteroid treatment and are currently in an acute phase of the disease
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 2 locations
1
Fondazione Policlinico Universitario A. Gemelli IRCCS
Roma, Italy, 00168
Not Yet Recruiting
2
Fondazione Policlinico Universitario Agostino Gemelli IRCCS
Rome, Italy, 00168
Actively Recruiting
Research Team
O
Ornella Parolini
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NON_RANDOMIZED
Model
PARALLEL
Primary Purpose
BASIC_SCIENCE
Number of Arms
3
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