Independent directory Public ClinicalTrials.gov records United States
ClinicalTrials.gov record
Completed No phase listed Observational

Impact of the BETACONNECT Auto-injector on BETASERON Therapy Adherence and Patient Satisfaction

ClinicalTrials.gov ID: NCT02652091

Public ClinicalTrials.gov record NCT02652091. 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 Sep 11, 2026, 5:22 AM EDT

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

Brief summary

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

The primary objective of this study is to assess adherence and persistence to BETASERON therapy in patients who are using the BETACONNECT auto-injector device (BETACONNECT device). The secondary objective of this study is to assess patient-reported satisfaction with the BETACONNECT device.

Study identification

NCT ID
NCT02652091
Recruitment status
Completed
Study type
Observational
Phase
Not listed
Lead sponsor
Bayer
Industry
Enrollment
146 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
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
Feb 4, 2016
Primary completion
Aug 10, 2017
Completion
Sep 12, 2017
Last update posted
Sep 5, 2018

2016 – 2017

United States locations

U.S. sites
23
U.S. states
14
U.S. cities
22
Facility City State ZIP Site status
Not listed Cullman Alabama 35058
Not listed Boca Raton Florida 33428
Not listed New Port Richey Florida 34653
Not listed Tampa Florida 33609
Not listed Atlanta Georgia 30309-1465
Not listed Fulton Maryland 20759
Not listed Foxborough Massachusetts 02035
Not listed Deckerville Michigan 48427
Not listed St Louis Missouri 63131
Not listed Stratford New Jersey 08084
Not listed Teaneck New Jersey 07666
Not listed Staten Island New York 10306
Not listed Medford Oregon 97504
Not listed Medford Oregon
Not listed Bala-Cynwyd Pennsylvania 19004
Not listed Lititz Pennsylvania 17543
Not listed Franklin Tennessee 37064
Not listed Memphis Tennessee 38104
Not listed Nashville Tennessee 37212
Not listed Lubbock Texas 79430
Not listed Round Rock Texas 78681
Not listed Fairfax Virginia 22031
Not listed Virginia Beach Virginia

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 NCT02652091, 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 Sep 5, 2018 · Synced Sep 11, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02652091 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →