Tuberous Sclerosis Complex Clinical Trials

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The EXOPULSE Study - a Database for Routine Follow-up of Clinical Outcomes

Status: Recruiting
Location: See location...
Intervention Type: Device
Study Type: Observational
SUMMARY

The objective is to explore the potential short and long-term impact of the EXOPULSE Mollii Suit and EXOPULSE Suit on subjects with CP, MS, stroke, fibromyalgia or other neurologic disorders which may cause such types of symptoms, and to identify high responders among the sub-categories of the diagnoses. The primary endpoint will be improvements in the Berg/Pediatric Balance Scale (BBS/PBS) as a measurement of balance and risk of falls.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 2
Healthy Volunteers: f
View:

• Diagnosed with CP, MS, stroke, fibromyalgia or other neurologic disorder that may cause such type of symptoms.

• Diagnosed \>6 months prior to inclusion in case of MS or stroke as well as \>1 month prior to inclusion in the case of fibromyalgia.

• Give written informed consent

• Cognitively able to understand and follow verbal and/or written instructions

• A minimum age of 2 years

Locations
Other Locations
Sweden
Ottobock Care Sverige
RECRUITING
Bergshamra
Contact Information
Primary
Milana Mileusnic, PhD
milana.mileusnic@ottobock.com
+43 6648415079
Backup
Sanna Dünesius, MSc
sanna.dunesius@ottobock.com
+46 706243064
Time Frame
Start Date: 2026-02-18
Estimated Completion Date: 2027-12-31
Participants
Target number of participants: 200
Sponsors
Leads: Exoneural Network AB

This content was sourced from clinicaltrials.gov