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NCT00952133 · ClinicalTrials.gov registry record · Phase 4
Efficacy of IV Palo With IV Dexamethasone vs IV Palo for Prevention of Immediate & Delayed PONV
A Phase 4 study, sponsored by NYU Langone Health.
- Completed
- Registry status
- Phase 4
- Development phase
- 118
- Enrollment target
NCT00952133: Completed Phase 4 study, sponsored by NYU Langone Health.
NCT00952133 is a Phase 4 study that has completed, run by NYU Langone Health. The registered enrollment target is 118 participants, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (77% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00952133, a Phase 4 study, has completed, sponsored by NYU Langone Health.
- COMPLETED
- Registry status
- Phase 4
- Development phase
- 118 participants
- Enrollment target
Study Summary
The purpose of this study is to determine if subjects who receive Palonosetron plus Dexamethasone have less post-operative nausea and vomiting (PONV) than those who receive Palonosetron alone.
Primary Outcome
A Complete Response (CR): defined as no nausea, no vomiting/retching, no rescue medication and no withdrawal of consent from the time of administration of the study drug(s) until 72 hours post emergence from anesthesia.
Interventions
- DRUG Palonosetron only
- DRUG Palonosetron with Dexamethasone
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 118 participants |
| Start Date | 2009-07 |
| Est. Completion | 2011-04 |
| Phase | Phase 4 |
What the finished NCT00952133 record still lists
NCT00952133 is an interventional study that assigns participants to a tested intervention. The registered 118 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 (77% lower).
The record links to 0 conditions, and to 2 interventions - of which Palonosetron only is the first listed.
NCT00952133 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00952133 about?
NCT00952133 is a clinical study titled "Efficacy of IV Palo With IV Dexamethasone vs IV Palo for Prevention of Immediate & Delayed PONV". The purpose of this study is to determine if subjects who receive Palonosetron plus Dexamethasone have less post-operative nausea and vomiting (PONV) than those who receive Palonosetron alone.
What is the current status of trial NCT00952133?
This trial is currently completed. It is a Phase 4 study. The enrollment target is 118 participants. The study started on 2009-07. Estimated completion is 2011-04.
What interventions are being tested in trial NCT00952133?
The interventions under investigation include: Palonosetron only (DRUG), Palonosetron with Dexamethasone (DRUG).
Who is sponsoring clinical trial NCT00952133?
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 NCT00952133's enrollment target sits among peer trials
118 713th of 2000 higher than 1,287 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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