Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| Name | Class |
|---|---|
| Sheba Medical Center | OTHER_GOV |
Not provided
Not provided
Not provided
This study aims to provide myriad of physiological parameters in patients admitted in an internal medicine department, and which are defined as being in an increased risk of clinical deterioration within the first 72-hours after admission. The investigators will also conduct a retrospective comparison between physiological changes in patients who did deteriorate to those who did not. This will form the basis for the development of an algorithm for early prediction and warning of physiological and clinical deterioration during the first 72-hours of admission.
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| non-invasive monitoring | Device | Prospective monitoring with retrospective big-data analysis |
|
| Measure | Description | Time Frame |
|---|---|---|
| Monitoring blood pressure changes in high-risk patients | The investigators will record blood pressure measurements using a non-invasive wireless monitoring device working continuously for 72 hours in high-risk patients. | 72 hours per individual |
| Measure | Description | Time Frame |
|---|---|---|
| Monitoring early heart rate changes in high-risk patients | The investigators will record heart rate using a non-invasive wireless monitoring device working continuously for 72 hours in high-risk patients. | 72 hours per individual |
| Monitoring respiratory rate changes in high-risk patients |
Not provided
Inclusion Criteria:
Exclusion Criteria:
Not provided
Not provided
Male and female patients 18 years and older admitted to the internal medicine department and are at high-risk for clinical deterioration during the first 72-hours after admission. The investigators anticipate it will include patients with acute and chronic cardio-respiratory disease, systemic infections, etc.
Not provided
| Name | Affiliation | Role |
|---|---|---|
| Gad Segal, MD | The Sheba Medical Center, Tel Hashomer, Ramat Gan, Israel | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| The Sheba Medical Center, Tel Hashomer | Ramat Gan | 52621 | Israel |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 35679119 | Derived | Itelman E, Shlomai G, Leibowitz A, Weinstein S, Yakir M, Tamir I, Sagiv M, Muhsen A, Perelman M, Kant D, Zilber E, Segal G. Assessing the Usability of a Novel Wearable Remote Patient Monitoring Device for the Early Detection of In-Hospital Patient Deterioration: Observational Study. JMIR Form Res. 2022 Jun 9;6(6):e36066. doi: 10.2196/36066. |
Not provided
Not provided
The investigators plan to publish the data in a way that will allow all readers to access the data collected and analyzed
Not provided
Not provided
Not provided
Not provided
Not provided
| ID | Term |
|---|---|
| D000075902 | Clinical Deterioration |
| ID | Term |
|---|---|
| D018450 | Disease Progression |
| D020969 | Disease Attributes |
| D010335 | Pathologic Processes |
| D013568 | Pathological Conditions, Signs and Symptoms |
Not provided
Not provided
Not provided
Not provided
Not provided
The investigators will record respiratory rate using a non-invasive wireless monitoring device working continuously for 72 hours in high-risk patients. |
| 72 hours per individual |
| Monitoring blood oxygen saturation changes in high-risk patients | The investigators will record blood oxygen saturation using a non-invasive wireless monitoring device working continuously for 72 hours in high-risk patients. | 72 hours per individual |
| Monitoring stroke volume changes in high-risk patients | The investigators will record stroke volume measurements using a non-invasive wireless monitoring device working continuously for 72 hours in high-risk patients. | 72 hours per individual |
| Monitoring cardiac output changes in high-risk patients | The investigators will record cardiac output measurements using a non-invasive wireless monitoring device working continuously for 72 hours in high-risk patients. | 72 hours per individual |