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NCT01191021 · ClinicalTrials.gov registry record · Phase 1
Monitoring Exhaled Propofol to Individualize General Anesthesia
A Phase 1 study of General Anesthesia, sponsored by University of California, San Francisco.
- Completed
- Registry status
- Phase 1
- Development phase
- 20
- Enrollment target
- 1
- Study location
NCT01191021: Completed Phase 1 study of General Anesthesia, sponsored by University of California, San Francisco.
NCT01191021 is a Phase 1 study of General Anesthesia that has completed, run by University of California, San Francisco. The registered enrollment target is 20 participants, below the 1,633-participant average among 4 other General Anesthesia trials with a reported enrollment target (99% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01191021, a Phase 1 study of General Anesthesia, has completed, sponsored by University of California, San Francisco.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 20 participants
- Enrollment target
- 1
- Study location
Study Summary
This trial investigates the relationship between concentrations of the anesthetic drug propofol in exhaled breath, blood and drug effect in volunteers undergoing general anesthesia. The main goal of this study is to develop a pharmacokinetic - and dynamic model for propofol in exhaled breath.
Conditions Studied
Interventions
- DRUG Propofol Anesthesia
Study Locations (1)
California
- Department of Anesthesia and Perioperative Care, UCSF - San Francisco
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 20 participants |
| Start Date | 2010-08 |
| Est. Completion | 2010-10 |
| Phase | Phase 1 |
What the finished NCT01191021 record still lists
NCT01191021 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 20 participants, a relatively small participant target, below the 1,633-participant average among 4 other General Anesthesia trials with a reported enrollment target (99% lower).
The record links to 1 condition, with General Anesthesia appearing as the primary indexed condition, and to 1 intervention - of which Propofol Anesthesia is the first listed.
NCT01191021 reports a single indexed study location in California.
Frequently Asked Questions
What is clinical trial NCT01191021 about?
NCT01191021 is a clinical study titled "Monitoring Exhaled Propofol to Individualize General Anesthesia". This trial investigates the relationship between concentrations of the anesthetic drug propofol in exhaled breath, blood and drug effect in volunteers undergoing general anesthesia. The main goal of this study is to develop a pharmacokinetic - and dynamic model for propofol in exhaled breath.
What is the current status of trial NCT01191021?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 20 participants. The study started on 2010-08. Estimated completion is 2010-10.
What conditions does trial NCT01191021 study?
This clinical trial studies the following conditions: General Anesthesia.
What interventions are being tested in trial NCT01191021?
The interventions under investigation include: Propofol Anesthesia (DRUG).
Who is sponsoring clinical trial NCT01191021?
This trial is sponsored by University of California, San Francisco, which has 1,713 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT01191021 being conducted?
This trial has 1 study location across California. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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