Multiple Sclerosis Clinical Trial

Endpoint Calibration for a Phase 2 Study of Lisinopril in Multiple Sclerosis

Summary

This study aims to calibrate the Multiple Sclerosis Functional Composite (MSFC) for home implementation in a phase 2 trial of lisinopril in multiple sclerosis. In this initial stage, participants are required to travel to the study site one day a week for three weeks to complete the MSFC. They are also required to complete the MSFC at home once weekly for three weeks using remote sensing technology and video conferencing.

View Eligibility Criteria

Eligibility Criteria

Inclusion Criteria:

Males and females between the ages of 18 and 64.
Documented informed consent
Documented diagnosis of RRMS via 2010 McDonald Criteria
Normal blood pressure at baseline: 90-140 mmHg systolic AND 60-90 mmHg diastolic
Baseline score of 0-5.5 on Kurtzke's Expanded Disability Status Scale (EDSS)
Availability of a person in the home who is physically able and willing to steady the subject if s/he loses balance during the walk test.

Exclusion Criteria:

Hypotensive at baseline: <90 mmHg systolic or <60 mmHg diastolic
Hypertensive at baseline: >140 mmHg systolic or >90 mmHg diastolic
Bradycardia at baseline: < 50 bpm

Study is for people with:

Multiple Sclerosis

Phase:

Phase 2

Estimated Enrollment:

20

Study ID:

NCT02369926

Recruitment Status:

Unknown status

Sponsor:

Transparency Life Sciences

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There is 1 Location for this study

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Icahn School of Medicine at Mount Sinai
New York New York, 10029, United States More Info
Tarah Gustafson
Contact
[email protected]
Fred Lublin, MD
Principal Investigator

How clear is this clinincal trial information?

Study is for people with:

Multiple Sclerosis

Phase:

Phase 2

Estimated Enrollment:

20

Study ID:

NCT02369926

Recruitment Status:

Unknown status

Sponsor:


Transparency Life Sciences

How clear is this clinincal trial information?

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