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NCT00239993 · ClinicalTrials.gov registry record · Phase 4
A Study to Evaluate the Impact of Using Warm Compress Prior to Daily Injections of Copaxone®
A Phase 4 study, sponsored by Teva Neuroscience.
- Completed
- Registry status
- Phase 4
- Development phase
- 50
- Enrollment target
NCT00239993: Completed Phase 4 study, sponsored by Teva Neuroscience.
NCT00239993 is a Phase 4 study that has completed, run by Teva Neuroscience. The registered enrollment target is 50 participants, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (90% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00239993, a Phase 4 study, has completed, sponsored by Teva Neuroscience.
- COMPLETED
- Registry status
- Phase 4
- Development phase
- 50 participants
- Enrollment target
Study Summary
This study is designed to compare skin reactions with or without the use of warm compress prior to performing a Copaxone® injection.
Interventions
- DRUG glatiramer acetate
- PROCEDURE Warm compress prior to injection of glatiramer acetate
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 50 participants |
| Start Date | 2005-08 |
| Est. Completion | 2006-02 |
| Phase | Phase 4 |
What the finished NCT00239993 record still lists
NCT00239993 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 50 participants, a relatively small participant target, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (90% lower).
The record links to 0 conditions, and to 2 interventions - of which glatiramer acetate is the first listed.
NCT00239993 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00239993 about?
NCT00239993 is a clinical study titled "A Study to Evaluate the Impact of Using Warm Compress Prior to Daily Injections of Copaxone®". This study is designed to compare skin reactions with or without the use of warm compress prior to performing a Copaxone® injection.
What is the current status of trial NCT00239993?
This trial is currently completed. It is a Phase 4 study. The enrollment target is 50 participants. The study started on 2005-08. Estimated completion is 2006-02.
What interventions are being tested in trial NCT00239993?
The interventions under investigation include: glatiramer acetate (DRUG), Warm compress prior to injection of glatiramer acetate (PROCEDURE).
Who is sponsoring clinical trial NCT00239993?
This trial is sponsored by Teva Neuroscience, which has 3 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT00239993's enrollment target sits among peer trials
50 1255th of 2000 higher than 678 of 2,000 other Phase 4 trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Phase 4 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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