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Emergencies clinical trials

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NCT ID: NCT05793697 Not yet recruiting - Clinical trials for Chronic Obstructive Pulmonary Disease

Assessment Of Different Scores In Predicting Outcome In AECOPD Patients In Emergency Department

Start date: May 3, 2023
Phase:
Study type: Observational [Patient Registry]

evaluate the value of different scores in predicting hospital mortality and Need for MV In patients presented to ED with AECOPD.

NCT ID: NCT05791253 Completed - Pain Clinical Trials

Pain Management in Primary Intervention of the Mobile Emergency and Resuscitation Service

DOLSMUR
Start date: March 9, 2023
Phase:
Study type: Observational

The aim of the study is to carry out an inventory of practices relating to the management of pain: its recognition, assessment and treatment.

NCT ID: NCT05789901 Recruiting - Breast Cancer Clinical Trials

The MARVIN Chatbots to Provide Information for Different Health Conditions

Start date: March 1, 2024
Phase: N/A
Study type: Interventional

This research is a continuation of a usability study with the MARVIN chatbot. The investigators aim to adapt the MARVIN chatbot to open it to other health domains (e.g. breast cancer) and populations (e.g. pharmacists). Therefore, this protocol constitutes a master research protocol that will englobe different research projects with individual chatbots. The investigators adopt an adaptive platform trial design, which will allow flexibility in handling multiple interventions adapted to different populations while retaining the characteristics of a platform trial design allowing early withdrawal of ineffective trial arms based on interim data (implementation outcomes) and introduction of new trial arms.

NCT ID: NCT05788523 Recruiting - Emergencies Clinical Trials

Prediction Of Serious Adverse Event in Emergency Department With dysKAlemia, Retrospective Study

PODKA-R
Start date: January 2, 2023
Phase:
Study type: Observational

Dyskalemia, hypo- and hyperkalemia are common in the emergency department and are associated with increased morbidity and mortality. The potential seriousness of dyskalemia results from the potential alteration of intracardiac conduction and the increase in cardiac rhythm disorders, all associated with a lethal risk. Given the aspecific symptoms of dyskalemia and the complex causal links to be acquired, it is difficult to judge the severity of the disorders in front of an initial clinical presentation of a patient in the emergency room, as the patient may present a serious condition during his stay in the emergency room, related to the dyskalemia and not prejudged at first. The ECG is recommended to judge the severity of the disorder, in association with the level of kalemia, but the electrical changes of its pattern in the context of dyskalemia are sometimes so fine that even the eye of the practitioner is not able to detect them. To date and to our knowledge, there is no tool for predicting the risk of RTA or death in dyskalemia. The existing studies on the subject, including ECGs, seek to detect dyskalemia and not its complications, and the proposed tools only take into account the ECG and not the clinical context of the patient.

NCT ID: NCT05788224 Recruiting - Clinical trials for Advanced Colorectal Cancer in Elderly Patient

The Management of Complicated Colo-rectal Cancer in Older Patients in the Emergency Setting: the CO-OLDER Study

CO-OLDER
Start date: May 1, 2022
Phase:
Study type: Observational

This is a multicenter observational study aimed to investigate the management of older patients aged 75 years old and over admitted to the emergency department with complicated colorectal cancer. The final endpoint is to report morbidity and mortality in this group of frail individuals according to the shift of incidence of colorectal cancer in geriatric patients, over 2 periods: before the COVID pandemic outbreak (11th March 2020) and after the 11th March, during the ongoing pandemic.

NCT ID: NCT05787665 Recruiting - Dyspnea Clinical Trials

Evaluation of the Impact of Lung Ultrasound on Mortality and Rehospitalization in Patients Admitted to the Emergency Department With Dyspnea

HOSPITALUS
Start date: June 16, 2023
Phase:
Study type: Observational

Dyspnea is a frequent reason for referral to emergency departments, leading to a 30-day mortality rate of up to 10% and a 3-month rehospitalization rate of over 30%. Multiple etiologies, as well as poor performance of clinical examination and chest radiography, lead to a diagnostic error rate of nearly 30% at the end of emergency department care. These diagnostic errors lead to rehospitalization and an excess mortality rate of more than 50% compared to patients with a correct initial diagnosis, which is explained in particular by the use of inappropriate therapies. Lung ultrasound is a rapid, non-irradiating, non-invasive, inexpensive, reproducible imaging test that can be used at the bedside. It has a better diagnostic performance than chest radiography, commonly performed in emergency departments.The immediate benefit of lung ultrasound for the most common diagnoses in emergency medicine has already been demonstrated. From an organizational point of view, a few studies have shown a benefit of lung ultrasound in reducing the time spent in emergency departments and the number of additional examinations necessary for the final diagnosis. However, there is no data in the literature on the longer term impact of its use in the emergency department. The primary objective is to evaluate the impact of performing lung ultrasound in terms of 3-month mortality and rehospitalization as part of the diagnostic process for patients admitted to the emergency department with dyspnea.

NCT ID: NCT05787548 Completed - Behavior, Health Clinical Trials

Reducing Emergency Department Utilization With an After Visit Summary Nudge Toward Alternative Care Options

Start date: April 3, 2023
Phase: N/A
Study type: Interventional

Decreasing utilization of the Emergency Department (ED) is a priority for the system. Often, ED visits can be avoided if patients contact Geisinger first to get appropriate direction for their concern or are otherwise better informed about reasons to visit the ED vs. urgent care or primary care facilities. The study team is working to reduce ED utilization by including additional information in adult outpatient After Visit Summaries (AVSs). The study will involve will involve A/B testing different AVS versions, including 1) a version that encourages patients to contact Geisinger via different contact methods, 2) a version that includes a map to the patient's closest ConvenientCare location and accompanying information about ConvenientCare, and 3) a version that includes a self-triage guide. A control group will receive the current standard AVS. Analysis results will be assessed to determine which version is most effective at reducing ED use.

NCT ID: NCT05783557 Not yet recruiting - Clinical trials for Hypertensive Emergency

A Study of Clevidipine Butyrate Injectable Emulsion in the Treatment of Hypertensive Emergency and Sub-emergency

Start date: May 1, 2023
Phase: Phase 3
Study type: Interventional

A randomized, double-blind, active-compared phase ะจ clinical trial to evaluate clevidipine butyrate injectable emulsion in the treatment of Hypertensive Emergency and Sub-emergency.

NCT ID: NCT05776953 Recruiting - Analgesia Clinical Trials

Evaluation of the Effects of Ketorolac Dose on Duration of Analgesia in Emergency Department (ED) Renal Colic Patients

Start date: December 21, 2023
Phase: Phase 4
Study type: Interventional

This is a prospective interventional study examining the effect of ketorolac at doses of 15mg versus 30 mg for duration of analgesia in emergency department patients with suspected renal colic.

NCT ID: NCT05773508 Recruiting - Emergencies Clinical Trials

Impact of Video Regulation Associated With an Emergency Kit on Night Hospitalizations of the Residents of Nursing Homes.

VisioR-EHPAD
Start date: March 6, 2023
Phase:
Study type: Observational

The aim is to evaluate the effectiveness of the device (emergency kit and video-medical control in emergency call centers) in reducing deep night hospitalizations of elderly people living in retirement homes.