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NCT03300674 · ClinicalTrials.gov registry record · Phase 4
Intravenous Lidocaine Randomized Comparative Effectiveness Trial
A Phase 4 study, sponsored by Montefiore Medical Center.
- Completed
- Registry status
- Phase 4
- Development phase
- 154
- Enrollment target
NCT03300674: Completed Phase 4 study, sponsored by Montefiore Medical Center.
NCT03300674 is a Phase 4 study that has completed, run by Montefiore Medical Center. The registered enrollment target is 154 participants, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (70% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT03300674, a Phase 4 study, has completed, sponsored by Montefiore Medical Center.
- COMPLETED
- Registry status
- Phase 4
- Development phase
- 154 participants
- Enrollment target
Study Summary
This is a randomized, double-blind, emergency department based, comparative effectiveness study of two medication for acute abdominal pain: intravenous lidocaine and intravenous hydromorphone. Patients will be enrolled during an emergency department visit and followed throughout their emergency department course and then by telephone 7 days later.
Primary Outcome
Participants were asked to describe their pain on a scale from 0 to 10 with 0= no pain and 10= the worst pain imaginable
Interventions
- DRUG Lidocaine
- DRUG Hydromorphone
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 154 participants |
| Start Date | 2018-01-10 |
| Est. Completion | 2018-08-28 |
| Phase | Phase 4 |
What the finished NCT03300674 record still lists
NCT03300674 is an interventional study that assigns participants to a tested intervention. The registered 154 participants enrollment target is mid-sized for trials with a published cap, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (70% lower).
The record links to 0 conditions, and to 2 interventions - of which Lidocaine is the first listed.
NCT03300674 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT03300674 about?
NCT03300674 is a clinical study titled "Intravenous Lidocaine Randomized Comparative Effectiveness Trial". This is a randomized, double-blind, emergency department based, comparative effectiveness study of two medication for acute abdominal pain: intravenous lidocaine and intravenous hydromorphone. Patients will be enrolled during an emergency department visit and followed throughout their emergency depa...
What is the current status of trial NCT03300674?
This trial is currently completed. It is a Phase 4 study. The enrollment target is 154 participants. The study started on 2018-01-10. Estimated completion is 2018-08-28.
What interventions are being tested in trial NCT03300674?
The interventions under investigation include: Lidocaine (DRUG), Hydromorphone (DRUG).
Who is sponsoring clinical trial NCT03300674?
This trial is sponsored by Montefiore Medical Center, which has 345 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT03300674's enrollment target sits among peer trials
154 528th of 2000 higher than 1,471 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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