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Trials / Completed

CompletedNCT01909492

Measurement of Relaxin Peptide in Multiple Sclerosis (MS)

Measurement of Relaxin in the Serum and Cerebrospinal Fluid of Subjects With and Without the Relapsing Form of Multiple Sclerosis

Status
Completed
Phase
Study type
Observational
Enrollment
30 (actual)
Sponsor
Providence Health & Services · Academic / Other
Sex
Female
Age
18 Years – 45 Years
Healthy volunteers
Not accepted

Summary

This study will evaluate relaxin (RLX) levels in patients with multiple sclerosis.

Detailed description

The goal of this study is to obtain baseline information on serum and cerebrospinal fluid (CSF) relaxin levels in patients with MS, as well as to further study RXFP-1 receptor binding affinity for RLX in patients with active and clinically stable MS.

Conditions

Interventions

TypeNameDescription
PROCEDUREBlood DrawPatients will provide a serum sample for research.
PROCEDURELumbar PuncturePatients will have a lumbar puncture to obtain CSF.

Timeline

Start date
2013-09-20
Primary completion
2023-10-05
Completion
2023-10-05
First posted
2013-07-26
Last updated
2025-06-22
Results posted
2025-06-22

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01909492. Inclusion in this directory is not an endorsement.

Measurement of Relaxin Peptide in Multiple Sclerosis (MS) (NCT01909492) · Clinical Trials Directory