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NCT03039881 · ClinicalTrials.gov registry record
Evaluation of Non-Invasive Respiratory Volume Monitor
A clinical trial, sponsored by Tufts Medical Center.
- Completed
- Registry status
- 150
- Enrollment target
NCT03039881 is a clinical trial that has completed, run by Tufts Medical Center. The registered enrollment target is 150 participants.
The verdict
NCT03039881 has completed, sponsored by Tufts Medical Center.
- COMPLETED
- Registry status
- 150 participants
- Enrollment target
Study Summary
This observational study investigates the validity and utility of a new, non-significant risk, FDA approved respiratory monitor, ExSpiron, in the perioperative course of patients undergoing elective surgery under general anesthesia. The study patients will be monitored before, during and after surgery, in post-anaesthesia care unit (PACU) and recovery room for the first post-operative night. The physiologic data will not be used or influence the standard of care for subjects. It is anticipated that this monitor may be able to improve perioperative care in the future.
Interventions
- DEVICE Non-Invasive Respiratory Volume Monitor
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 150 participants |
| Start Date | 2015-01-09 |
| Est. Completion | 2019-01-08 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT03039881
The ClinicalTrials.gov registry entry for NCT03039881 describes a study currently listed as completed, categorized as an unspecified phase. The registered enrollment target is 150 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Tufts Medical Center, which has 169 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 1 intervention - of which Non-Invasive Respiratory Volume Monitor is the first listed.
NCT03039881 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT03039881 about?
NCT03039881 is a clinical study titled "Evaluation of Non-Invasive Respiratory Volume Monitor". This observational study investigates the validity and utility of a new, non-significant risk, FDA approved respiratory monitor, ExSpiron, in the perioperative course of patients undergoing elective surgery under general anesthesia. The study patients will be monitored before, during and after surge...
What is the current status of trial NCT03039881?
This trial is currently completed. The enrollment target is 150 participants. The study started on 2015-01-09. Estimated completion is 2019-01-08.
What interventions are being tested in trial NCT03039881?
The interventions under investigation include: Non-Invasive Respiratory Volume Monitor (DEVICE).
Who is sponsoring clinical trial NCT03039881?
This trial is sponsored by Tufts Medical Center, which has 169 total clinical trials registered on ClinicalTrials.gov.
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