Assessing Tolerability of Avonex Intramuscular Injections
Completed · Not applicable
Conditions studied: Multiple Sclerosis
In brief
The purpose of this study is to evaluate patients' views when injecting Avonex intramuscularly.
Key facts
- Study ID
- NCT01641120
- Run by
- Trinity Health Of New England
- People needed
- 20
- Starts
- 2012-05-01
- Expected to finish
- 2014-02-01
- Last updated by the study team
- 2016-02-01
Who can join
Age: 18 and older, up to 65. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Between 18 - 65 years of age;
- Confirmed diagnosis of Relapsing Remitting Multiple Sclerosis;
- Currently being treated with Avonex® for at least 90 days;
- Using 25 gauge needles for injection of Avonex® for at least 90 days;
- Willing and able to complete study questionnaires; and
- Provided informed consent to participate in this study
You may not qualify if…
- Diagnosis of Progressive Multiple Sclerosis;
- History of recent illness or infection;
- History of allergic reaction to Avonex®;
- Any prior usage of a 30 gauge needle for administration of Avonex®;
- Concurrent treatment with other immunomodulating therapies;
- Pregnant or planning on becoming pregnant;
- Nursing mothers; and
- Unable to complete the requirements of the study
Where it is running
- The Mandell Center for Multiple Sclerosis — Hartford, Connecticut, United States
Full record on ClinicalTrials.gov
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