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NCT02630134 · ClinicalTrials.gov registry record · NA
Device for Monitoring Pain During Intraoperative, Pre/Post Surgical Periods: Comparison With Standard of Care Monitoring
A NA study, sponsored by NYU Langone Health.
- Terminated
- Registry status
- NA
- Development phase
- 6
- Enrollment target
NCT02630134: Clinical Trial NA study, sponsored by NYU Langone Health.
NCT02630134 is a NA study that was terminated before completion, run by NYU Langone Health. The registered enrollment target is 6 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (100% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT02630134, a NA study, was terminated before completion, sponsored by NYU Langone Health.
- TERMINATED
- Registry status
- NA
- Development phase
- 6 participants
- Enrollment target
Study Summary
Study patients are given a hand held device to track pain post surgery.
Primary Outcome
VAS score 0-10
Interventions
- OTHER These patients receive the Baeta device and take it home
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 6 participants |
| Start Date | 2011-03 |
| Est. Completion | 2012-10 |
| Phase | NA |
Why NCT02630134 stopped before completion
NCT02630134 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 6 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (100% lower).
The record links to 0 conditions, and to 1 intervention - of which These patients receive the Baeta device and take it home is the first listed.
NCT02630134 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT02630134 about?
NCT02630134 is a clinical study titled "Device for Monitoring Pain During Intraoperative, Pre/Post Surgical Periods: Comparison With Standard of Care Monitoring". Study patients are given a hand held device to track pain post surgery.
What is the current status of trial NCT02630134?
This trial is currently terminated. It is a NA study. The enrollment target is 6 participants. The study started on 2011-03. Estimated completion is 2012-10.
What interventions are being tested in trial NCT02630134?
The interventions under investigation include: These patients receive the Baeta device and take it home (OTHER).
Who is sponsoring clinical trial NCT02630134?
This trial is sponsored by NYU Langone Health, which has 1,164 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT02630134's enrollment target sits among peer trials
6 1983rd of 2000 higher than 13 of 2,000 other NA trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other NA 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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