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NCT06289699 · ClinicalTrials.gov registry record
Alert Frequency, Nurse, and Patient Satisfaction With a wCVSM Software Across Health Care Systems and Cultures
A clinical trial of Postoperative Complications and Acute Medical Conditions, sponsored by Christian S. Meyhoff.
- Recruiting
- Registry status
- 100
- Enrollment target
- 5
- Study locations
NCT06289699: Recruiting study of Postoperative Complications and Acute Medical Conditions, sponsored by Christian S. Meyhoff.
NCT06289699 is a study of Postoperative Complications and Acute Medical Conditions that is actively recruiting participants, run by Christian S. Meyhoff. The registered enrollment target is 100 participants, below the 557-participant average among 20 other Postoperative Complications trials with a reported enrollment target (82% lower). The trial reports 5 study locations across 2 states. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT06289699, a study of Postoperative Complications and Acute Medical Conditions, is actively recruiting participants, sponsored by Christian S. Meyhoff.
- RECRUITING
- Registry status
- 100 participants
- Enrollment target
- 5
- Study locations
Study Summary
The goal of this prospective, international multi-centre pilot study is to assess the functionality and user experience of a new vital sign monitoring system in 20 patients and 20 nurses in the general ward at each centre. The patients will be monitored with a wireless, continuous vital sign monitoring systems and answer a questionnaire afterwards. They will in addition have vital signs monitored as per standard practice. The nurses will answer a questionnaire after having had the responsibility for a monitored patient for a full shift. The main aims are: To determine the frequency of alerts activated in the app in relation to the alerts that should be activated based on measured data, to explore current practices of in-hospital monitoring by semi-structured interviews to map differences across systems and to test nurse and patient satisfaction.
Conditions Studied
Study Locations (5)
Other
- Universitätsklinikum Hamburg-Eppendorf (UKE), Zentrum für Anästhesiologie und Intensivmedizin, Klinik und Poliklinik für Anästhesiologie - Hamburg
- University Medical Center Groningen, Department of Anesthesiology - Groningen
- St. Olavs Hospital HF, Klinikk for anestesi og intensivmedisin - Trondheim
- Liverpool University Hospitals NHS Foundation Trust - Liverpool
Ohio
- The Cleveland Clinic Foundation, General Anesthesiology - Cleveland
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 100 participants |
| Start Date | 2024-02-26 |
| Est. Completion | 2026-12-31 |
What NCT06289699 shows while recruiting
NCT06289699 is an observational study that tracks outcomes without assigning an intervention. The registered 100 participants enrollment target is mid-sized for trials with a published cap, below the 557-participant average among 20 other Postoperative Complications trials with a reported enrollment target (82% lower).
The record links to 3 conditions, with Postoperative Complications appearing as the primary indexed condition, and to 0 interventions.
NCT06289699 lists 5 locations in 2 states (Other, Ohio).
Frequently Asked Questions
What is clinical trial NCT06289699 about?
NCT06289699 is a clinical study titled "Alert Frequency, Nurse, and Patient Satisfaction With a wCVSM Software Across Health Care Systems and Cultures". The goal of this prospective, international multi-centre pilot study is to assess the functionality and user experience of a new vital sign monitoring system in 20 patients and 20 nurses in the general ward at each centre. The patients will be monitored with a wireless, continuous vital sign monitor...
What is the current status of trial NCT06289699?
This trial is currently recruiting. The enrollment target is 100 participants. The study started on 2024-02-26. Estimated completion is 2026-12-31.
What conditions does trial NCT06289699 study?
This clinical trial studies the following conditions: Postoperative Complications, Acute Medical Conditions, User Experience.
Who is sponsoring clinical trial NCT06289699?
This trial is sponsored by Christian S. Meyhoff, which has 1 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06289699 being conducted?
This trial has 5 study locations across Ohio. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
Similar trials for Postoperative Complications
Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.
Where NCT06289699's enrollment target sits among peer trials
100 12th of 20 higher than 6 of 20 other Postoperative Complications trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Postoperative Complications 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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