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NCT07216573 · ClinicalTrials.gov registry record · NA
The Continuity Study
A NA study, sponsored by Becton, Dickinson and Company.
- Recruiting
- Registry status
- NA
- Development phase
- 188
- Enrollment target
NCT07216573 is a NA study that is actively recruiting participants, run by Becton, Dickinson and Company. The registered enrollment target is 188 participants.
The verdict
NCT07216573, a NA study, is actively recruiting participants, sponsored by Becton, Dickinson and Company.
- RECRUITING
- Registry status
- NA
- Development phase
- 188 participants
- Enrollment target
Study Summary
A before and after interventional cohort study comparing intermittent blood pressure measurement using the oscillometric arm cuff to continuous noninvasive blood pressure (cNIBP) measurement using the VitaWave finger cuffs in subjects undergoing elective surgery in an outpatient setting.
Interventions
- DEVICE HemoSphere Vita Monitor with VitaWave or VitaWave Plus Finger Cuff Adult, and ForeSight Large Sensors
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 188 participants |
| Start Date | 2026-05-07 |
| Est. Completion | 2027-02 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT07216573
The ClinicalTrials.gov registry entry for NCT07216573 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 188 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Becton, Dickinson and Company, which has 33 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 1 intervention - of which HemoSphere Vita Monitor with VitaWave or VitaWave Plus Finger Cuff Adult, and ForeSight Large Sensors is the first listed.
NCT07216573 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT07216573 about?
NCT07216573 is a clinical study titled "The Continuity Study". A before and after interventional cohort study comparing intermittent blood pressure measurement using the oscillometric arm cuff to continuous noninvasive blood pressure (cNIBP) measurement using the VitaWave finger cuffs in subjects undergoing elective surgery in an outpatient setting.
What is the current status of trial NCT07216573?
This trial is currently recruiting. It is a NA study. The enrollment target is 188 participants. The study started on 2026-05-07. Estimated completion is 2027-02.
What interventions are being tested in trial NCT07216573?
The interventions under investigation include: HemoSphere Vita Monitor with VitaWave or VitaWave Plus Finger Cuff Adult, and ForeSight Large Sensors (DEVICE).
Who is sponsoring clinical trial NCT07216573?
This trial is sponsored by Becton, Dickinson and Company, which has 33 total clinical trials registered on ClinicalTrials.gov.
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