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Completed No phase listed Observational

Real-World Betaseron Health Economic Outcomes Study for Relapsing Forms of Multiple Sclerosis

ClinicalTrials.gov ID: NCT01158183

Public ClinicalTrials.gov record NCT01158183. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 22, 2026, 12:43 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Real-World Betaseron® Outcomes Study (ROBUST): A Twelve-month, US Prospective, Observational, Open-label, Single-arm, Multi-center Outcomes Study of Interferon β-1b (Betaseron®) Given Every Other Day for Relapsing Forms of Multiple Sclerosis

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

A Web based real world observational study in Relapsing-Remitting Multiple Sclerosis (RRMS) population capturing outcomes reported by patients and by the physicians during 12 months after initiating or resuming Betaseron.

Study identification

NCT ID
NCT01158183
Recruitment status
Completed
Study type
Observational
Phase
Not listed
Lead sponsor
Bayer
Industry
Enrollment
226 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 65 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jul 2007 (Type not available)
Primary completion
Sep 2009 (Actual)
Completion
Sep 2009 (Actual)
Last update posted
Jul 8, 2010

2007 – 2009

United States locations

U.S. sites
27
U.S. states
27
U.S. cities
27
Facility City State ZIP Site status
Not listed Many Locations Alabama — —
Not listed Many Locations California — —
Not listed Many Locations Colorado — —
Not listed Many Locations Florida — —
Not listed Many Locations Illinois — —
Not listed Many Locations Iowa — —
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Not listed Many Locations New Hampshire — —
Not listed Many Locations New Jersey — —
Not listed Many Locations New York — —
Not listed Many Locations North Carolina — —
Not listed Many Locations North Dakota — —
Not listed Many Locations Ohio — —
Not listed Many Locations Oregon — —
Not listed Many Locations Pennsylvania — —
Not listed Many Locations Rhode Island — —
Not listed Many Locations Tennessee — —
Not listed Many Locations Texas — —
Not listed Many Locations Virginia — —
Not listed Many Locations Washington — —
Not listed Many Locations Wisconsin — —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01158183, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jul 8, 2010 · Synced Oct 22, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01158183 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →