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NCT00689130 · ClinicalTrials.gov registry record
ADVANCE: Assessment for Defining Variability in Anesthesia Through Novel Clinical EEG
A clinical trial, sponsored by Medtronic - MITG.
- Completed
- Registry status
- 120
- Enrollment target
NCT00689130: Completed study, sponsored by Medtronic - MITG.
NCT00689130 is a clinical trial that has completed, run by Medtronic - MITG. The registered enrollment target is 120 participants. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00689130 has completed, sponsored by Medtronic - MITG.
- COMPLETED
- Registry status
- 120 participants
- Enrollment target
Study Summary
The present study is designed to compare prospectively whether sBIS, sEMG, or CVI variability (brain monitoring) can be used to predict unwanted intraoperative responses (high blood pressure, fast heart rate, tearing, etc.) to stimulation (pain) and to determine whether these intraoperative findings are related to patient-assessed postoperative pain scores. The hypothesis is that increases in these variability measures are associated with increased probability of unwanted responses. If confirmed, these variability measures may help anesthesia providers by highlighting periods of inadequate analgesia (pain relief).
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 120 participants |
| Start Date | 2008-05 |
| Est. Completion | 2008-10 |
What the finished NCT00689130 record still lists
NCT00689130 is an observational study that tracks outcomes without assigning an intervention. The registered 120 participants enrollment target is mid-sized for trials with a published cap.
The record links to 0 conditions, and to 0 interventions.
NCT00689130 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00689130 about?
NCT00689130 is a clinical study titled "ADVANCE: Assessment for Defining Variability in Anesthesia Through Novel Clinical EEG". The present study is designed to compare prospectively whether sBIS, sEMG, or CVI variability (brain monitoring) can be used to predict unwanted intraoperative responses (high blood pressure, fast heart rate, tearing, etc.) to stimulation (pain) and to determine whether these intraoperative findings...
What is the current status of trial NCT00689130?
This trial is currently completed. The enrollment target is 120 participants. The study started on 2008-05. Estimated completion is 2008-10.
Who is sponsoring clinical trial NCT00689130?
This trial is sponsored by Medtronic - MITG, which has 119 total clinical trials registered on ClinicalTrials.gov.
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