Deterioration, Clinical

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Review clinical trials related to Deterioration, Clinical. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

Cognitive Outcomes in BAD-related Stroke

Branch atheromatous disease (BAD) is a distinct subtype of ischemic stroke that is particularly prevalent among Chinese and other Asian populations. Patients with BAD are prone to early neurological deterioration and poor functional outcomes, and BAD is increasingly recognized as an independent disease entity. However, the association between BAD and cognitive impairment remains unclear. This nationwide, multicenter, prospective observational study will prospectively collect epidemiological, clinical, neuroimaging, functional, and cognitive outcome data from patients with BAD. The study aims to investigate the occurrence of cognitive impairment after BAD and identify the clinical and neuroimaging characteristics associated with cognitive impairment. In particular, the relationship between early neurological deterioration (END) and cognitive impairment will be investigated. As an exploratory objective, this study will further explore the potential brain network mechanisms underlying cognitive impairment associated with END events.

Participants needed: 60
Trial details
Age: 18-80Biological sex: AllType: ObservationalSponsor: Peking Union Medical College HospitalUpdated: Aug 12, 2026Locations: 1
Eligibility criteria

Age: 18-80 years. [+1]

Baseline imaging showing intracranial hemorrhagic disease, vascular malformation... [+7]

Status: Recruiting

Clinical Assessment and Treatment in the Nursing Home as an Alternative to Hospital Admission

This multicenter, cluster-randomized, unblinded quality-improvement study evaluates whether home-based clinical assessment by municipal acute care teams can safely reduce hospital admissions among nursing home residents experiencing acute illness or clinical deterioration during out-of-hours periods. Participating nursing homes in the Capital Region of Denmark will be randomized to either usual care (contacting the regional medical helpline, 1813) or the intervention pathway, in which nursing home staff contact a municipal acute care team directly. The acute care team performs an on-site clinical assessment and, when needed, consults a senior physician in the hospital emergency department to establish a treatment and observation plan, which may include continued management at the nursing home under hospital responsibility. The study compares the intervention with usual care with respect to hospital admissions and mortality among nursing home residents.

Participants needed: 9,000
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Copenhagen University Hospital at HerlevUpdated: Aug 10, 2026Locations: 4
Eligibility criteria

Nursing homes, defined as long-term care facilities with care personnal availabl... [+2]

Assisted living facilities, intermediate/temporary care units, rehabilitation un... [+1]

Status: Not yet recruiting

Optimized Novel Wireless Assessment of Respiratory and Circulatory Dirstress - Alarm Validation

The ONWARD study evaluates user experiences from continuous vital sign monitoring alarms sent to the clinical staff in case of deviating vital signs at the general hospital ward. User experiences are evaluated though a 5-point likert questionnaire.

Participants needed: 100
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Eske Kvanner AasvangUpdated: Jun 16, 2026Locations: 2
Eligibility criteria

Age ≥ 18 years [+2]

Having implanted electronic devices (such as pacemaker or Implantable Cardiovert... [+3]

Status: Recruiting

Adverse Outcome of Acute Pulmonary Embolism by Artificial Intelligence System Based on CT Pulmonary Angiography

The investigators aim to build a predictive tool for Adverse Outcome of Acute Pulmonary Embolism by Artificial Intelligence System Based on CT Pulmonary Angiography.

Participants needed: 2,000
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Shengjing HospitalUpdated: Mar 11, 2026Locations: 1
Eligibility criteria

age of ≥ 18 years and a pulmonary embolism diagnosis based on CT pulmonary angio...

pregnancy [+2]

Status: Recruiting

A Predictive Tool for Predicting Adverse Outcomes in Acute Pulmonary Embolism Patients Using CTPA.

This study collected clinical, laboratory, and CT parameters of acute patients with acute pulmonary embolism from admission to predict adverse outcomes within 30 days after admission into hospital.

Participants needed: 300
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Shengjing HospitalUpdated: Mar 11, 2026Locations: 1Duration: 30 Days
Eligibility criteria

age of ≥ 18 years and a PE diagnosis based on CT pulmonary angiography

pregnancy [+2]

Status: Recruiting

Feasibility and Initial Clinical Impressions of Predictive Monitoring Integrated With the RACE Team

Rapid response teams (RRTs) have been adopted by hospitals to provide urgent critical care to hospitalized patients who require quick intervention to prevent further deterioration. Early warning scores (EWS) serve as a method to identify patients requiring RRT assessment by analyzing routinely collected data such as vital signs and laboratory results. The Visensia Safety Index (VSI) is an EWS that uses continuous vital sign monitoring and machine learning to identify the likelihood of deterioration and can be integrated with existing hospital data infrastructure. Initial studies of the VSI have both validated the system and found that patients monitored using VSI had a shorter duration of any instability and fewer episodes of serious and persistent instability. The investigators' recent retrospective analysis at The Ottawa Hospital (TOH) identified that implementation of an EWS could have detected earlier deterioration in over half of the patients identified, potentially preventing subsequent ICU admission, severity of illness, and/or mortality. Thus, this study aims to determine the feasibility and potential impact of implementing a portable continuous monitoring system with a VSI trigger at TOH to identify patients at high risk of deterioration.

Participants needed: 140
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Ottawa Hospital Research InstituteUpdated: May 14, 2025Locations: 1
Eligibility criteria

Patients who have undergone high risk elective surgery (Whipple procedures, high... [+3]

Patients admitted to a unit with higher level monitoring (Neurological Acute Ass... [+1]