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NCT00747916 · ClinicalTrials.gov registry record · Phase 4
Safety, Efficacy, and Side Effects Study of Interventional Cryotherapy in the Pleural Space("ICE PLS")
A Phase 4 study, sponsored by CSA Medical.
- Terminated
- Registry status
- Phase 4
- Development phase
- 3
- Enrollment target
NCT00747916: Clinical Trial Phase 4 study, sponsored by CSA Medical.
NCT00747916 is a Phase 4 study that was terminated before completion, run by CSA Medical. The registered enrollment target is 3 participants, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (99% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00747916, a Phase 4 study, was terminated before completion, sponsored by CSA Medical.
- TERMINATED
- Registry status
- Phase 4
- Development phase
- 3 participants
- Enrollment target
Study Summary
The purpose of this study is to evaluate the safety, efficacy, and side effects of the CryoSpray Ablation(TM) System (CSA(TM) System) to treat neoplastic lesions on the parietal pleural surface.
Interventions
- DEVICE CryoSpray Ablation (TM) System
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 3 participants |
| Start Date | 2008-08 |
| Est. Completion | 2009-08 |
| Phase | Phase 4 |
Why NCT00747916 stopped before completion
NCT00747916 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 3 participants, a relatively small participant target, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (99% lower).
The record links to 0 conditions, and to 1 intervention - of which CryoSpray Ablation (TM) System is the first listed.
NCT00747916 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00747916 about?
NCT00747916 is a clinical study titled "Safety, Efficacy, and Side Effects Study of Interventional Cryotherapy in the Pleural Space("ICE PLS")". The purpose of this study is to evaluate the safety, efficacy, and side effects of the CryoSpray Ablation(TM) System (CSA(TM) System) to treat neoplastic lesions on the parietal pleural surface.
What is the current status of trial NCT00747916?
This trial is currently terminated. It is a Phase 4 study. The enrollment target is 3 participants. The study started on 2008-08. Estimated completion is 2009-08.
What interventions are being tested in trial NCT00747916?
The interventions under investigation include: CryoSpray Ablation (TM) System (DEVICE).
Who is sponsoring clinical trial NCT00747916?
This trial is sponsored by CSA Medical, which has 9 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT00747916's enrollment target sits among peer trials
3 1995th of 2000 higher than 3 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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