Efficacy of Transcranial Static Magnetic Field Stimulation (tSMS) and Potential Theranostic Biomarkers in Amyotrophic Lateral Sclerosis (ALS).

Status: Recruiting
Location: See location...
Intervention Type: Device
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

The objective of the present study is to assess the efficacy of tSMS in ALS patients. This will be achieved by monitoring: * levels of NF-L and other potential innovative biomarkers, * clinical progression, trough ALSFRS-R. After at least three-month follow-up, participants will be recruited to undergo biemispheric tSMS for two daily sessions of 120 minutes each, at home, for 12 months. Together with clinical status, which will be evalueted each three months, blood and urine samples will be collected before the start of the tSMS administration (M0) and during the treatment (M3, M6, M9, M12), to detect potential theranostic biomarkers. In a subgroup of patients, ad additional blood and urine sample will be collected 3 months before M0 (M-3). Moreover, cortical excitability will be tested through transcranial magnetic stimulation (TMS) before and after the tSMS stimulation period.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• age ≥ 18

• diagnosis of possible, probable or definite ALS according to revised El Escorial criteria and Awaji-Shima criteria

• disease duration \< 24 months

• ALSFRS-R \> 30 at the recruitment

• ALSFRS-R decline \> 1 in the at least 3-months period before the intervention

• normal respiratory functionality at the preliminary evaluation (M-3), assessed in the previous month (FVC ≥ 75% and ALSFRS-R items 10,11,12 \> 4)

• treatment with riluzole 50 mg x 2/die

Locations
Other Locations
Italy
Fondazione Policlinico Campus Bio-Medico
RECRUITING
Roma
Contact Information
Primary
Vincenzo Di Lazzaro
v.dilazzaro@policlinicocampus.it
06 22541 1220
Time Frame
Start Date: 2024-12-02
Estimated Completion Date: 2027-12-31
Participants
Target number of participants: 60
Treatments
Experimental: pwALS
All participants will undergo tSMS administration at home, in two daily sessions of 120 minutes each.
Sponsors
Leads: Campus Bio-Medico University

This content was sourced from clinicaltrials.gov