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NCT02240628 · ClinicalTrials.gov registry record · Phase 4
Combining Placing a Synera Patch With Propofol/Lidocaine Mixture to Decrease Pain With IV Propofol Injection
A Phase 4 study, sponsored by The University of Texas Health Science Center, Houston.
- Completed
- Registry status
- Phase 4
- Development phase
- 76
- Enrollment target
NCT02240628: Completed Phase 4 study, sponsored by The University of Texas Health Science Center, Houston.
NCT02240628 is a Phase 4 study that has completed, run by The University of Texas Health Science Center, Houston. The registered enrollment target is 76 participants, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (85% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT02240628, a Phase 4 study, has completed, sponsored by The University of Texas Health Science Center, Houston.
- COMPLETED
- Registry status
- Phase 4
- Development phase
- 76 participants
- Enrollment target
Study Summary
The main objective is to evaluate if combining placing the Synera patch and using Propofol /Lidocaine mixture will further decrease the pain associated with the IV injection of Propofol.
Interventions
- DRUG Saline
- DRUG Lidocaine
- DEVICE Lidocaine/tetracaine transdermal patch
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 76 participants |
| Start Date | 2014-08 |
| Est. Completion | 2015-09 |
| Phase | Phase 4 |
What the finished NCT02240628 record still lists
NCT02240628 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 76 participants, a relatively small participant target, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (85% lower).
The record links to 0 conditions, and to 3 interventions - of which Saline is the first listed.
NCT02240628 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT02240628 about?
NCT02240628 is a clinical study titled "Combining Placing a Synera Patch With Propofol/Lidocaine Mixture to Decrease Pain With IV Propofol Injection". The main objective is to evaluate if combining placing the Synera patch and using Propofol /Lidocaine mixture will further decrease the pain associated with the IV injection of Propofol.
What is the current status of trial NCT02240628?
This trial is currently completed. It is a Phase 4 study. The enrollment target is 76 participants. The study started on 2014-08. Estimated completion is 2015-09.
What interventions are being tested in trial NCT02240628?
The interventions under investigation include: Saline (DRUG), Lidocaine (DRUG), Lidocaine/tetracaine transdermal patch (DEVICE).
Who is sponsoring clinical trial NCT02240628?
This trial is sponsored by The University of Texas Health Science Center, Houston, which has 732 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT02240628's enrollment target sits among peer trials
76 994th of 2000 higher than 999 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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