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NCT01219881 · ClinicalTrials.gov registry record · Phase 3
Comparing Desflurane to Sevoflurane for the Effect on Recovery Time in Patients Undergoing Urological Cystoscope Surgery
A Phase 3 study, sponsored by Ohio State University.
- Completed
- Registry status
- Phase 3
- Development phase
- 75
- Enrollment target
NCT01219881: Completed Phase 3 study, sponsored by Ohio State University.
NCT01219881 is a Phase 3 study that has completed, run by Ohio State University. The registered enrollment target is 75 participants, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (90% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01219881, a Phase 3 study, has completed, sponsored by Ohio State University.
- COMPLETED
- Registry status
- Phase 3
- Development phase
- 75 participants
- Enrollment target
Study Summary
This is a single-center, prospective, randomized, double-blind, double-arm trial including 68 subjects scheduled to undergo urological cystoscope surgeries under general anesthesia (GA) with intubation through a laryngeal mask airway (LMA) at The Ohio State University Medical Center (OSUMC). Double blinding will be based on both the subject and the research staff being unaware of which trial arm the subject is randomized into. Eligible subjects that provide voluntary and written informed consent will be included in this study.
Primary Outcome
Recovery Time after exposure to desflurane or sevoflurane considering time of emergence from anesthesia
Interventions
- DRUG Sevoflurane
- DRUG Desflurane
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 75 participants |
| Start Date | 2010-09 |
| Est. Completion | 2012-10 |
| Phase | Phase 3 |
What the finished NCT01219881 record still lists
NCT01219881 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 75 participants, a relatively small participant target, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (90% lower).
The record links to 0 conditions, and to 2 interventions - of which Sevoflurane is the first listed.
NCT01219881 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT01219881 about?
NCT01219881 is a clinical study titled "Comparing Desflurane to Sevoflurane for the Effect on Recovery Time in Patients Undergoing Urological Cystoscope Surgery". This is a single-center, prospective, randomized, double-blind, double-arm trial including 68 subjects scheduled to undergo urological cystoscope surgeries under general anesthesia (GA) with intubation through a laryngeal mask airway (LMA) at The Ohio State University Medical Center (OSUMC). Double ...
What is the current status of trial NCT01219881?
This trial is currently completed. It is a Phase 3 study. The enrollment target is 75 participants. The study started on 2010-09. Estimated completion is 2012-10.
What interventions are being tested in trial NCT01219881?
The interventions under investigation include: Sevoflurane (DRUG), Desflurane (DRUG).
Who is sponsoring clinical trial NCT01219881?
This trial is sponsored by Ohio State University, which has 552 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT01219881's enrollment target sits among peer trials
75 1773rd of 2000 higher than 221 of 2,000 other Phase 3 trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Phase 3 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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