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Length of Stay clinical trials

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NCT ID: NCT03751319 Completed - Quality of Life Clinical Trials

Geriatric Assessment and Intervention for Older Patients With Frailty in the Emergency Department

GAOPS
Start date: December 11, 2018
Phase: N/A
Study type: Interventional

Comprehensive Geriatric Assessment (CGA) is an established approach for better detection of frailty-related problems and includes individualized treatment plan with multi-discipline supportive and treating measures for the older frailty patients. However, there is limited evidence of feasibility and efficacy of the CGA when provided in the emergency department setting. In the GAOPS-study the efficacy of the CGA in emergency department setting will be studied by randomized controlled study protocol. We aim to study if the CGA provided in the ED is feasible, safe and efficient method when added with standard emergency care for older frail patients.

NCT ID: NCT03665987 Not yet recruiting - Clinical trials for Postoperative Complications

The Effect of Preoperative Assessment Clinic on Prognosis and Economic Results of Patients With Coexisting Disease.

Start date: October 1, 2018
Phase:
Study type: Observational [Patient Registry]

To assess the effect of preoperative assessment clinic on prognosis and economic results of patients with coexisting diseases, the investigators designed a prospective cohort study. The investigators will recruit 250 patients preparing to undergo a selective epigastrium surgery with coexisting medical diseases which need an anesthetic consultation. The patients will be randomly assigned into two groups. The intervention group will be seen in the preoperative clinic before hospitalization, while the control group will get anesthetic consultation after hospitalization without clinic service. No additional interventions will be given during and after surgery. The length of stay, hospitalization expense, postoperative complication rate and mortality rate of the two groups will be compared. The investigator assume that consultation in preoperative assessment clinic will improve the prognosis and decrease the hospitalization expenses.

NCT ID: NCT03633240 Recruiting - Emergencies Clinical Trials

Emergency Room Visits and Older Patients (ER2)

ER2
Start date: September 1, 2017
Phase:
Study type: Observational

Today's population is living longer than prior generations. Senior patients, defined as 65 years or older, are therefore increasing in number, and representing a larger number of hospitalized patients. Thus, assessing and addressing the needs of the growing number of older ER users is essential. The overall objective of the study is to examine the feasibility and the epidemiology of two screening tools ("Programme de Recherche sur l'Intégration des Services pour le Maintien de l'Autonomie" (PRISMA-7) and Emergency Room Evaluation and recommendations (ER2)) used in the Emergency Room of Jewish General Hospital to screen older patients (i.e.; ≥65 years) at risk of adverse health events. A prospective observational cohort design will be used for the study's two phases; phase 1- assessment and phase 2- assessment as well as recommendations.

NCT ID: NCT03527992 Recruiting - Pneumonia Clinical Trials

Automated Oxygen Administration in Patients With Hypoxemic Pneumonia and Pleuropneumonia

OPPAÎ
Start date: March 9, 2018
Phase: N/A
Study type: Interventional

Hypoxemic pneumonia is a major cause of hospitalization in Pulmonology. The patient's dependency on oxygen prevents early discharge from the hospital. An automated oxygen therapy is a system that allows administration of oxygen with a flow that is automatically adjusted to the patient's saturation, which is continuously monitored. This system has proven to be particularly effective with chronic obstructive pulmonary disease (COPD) patients, by decreasing the time spent in hypoxia and hyperoxia, and by accelerating the weaning of oxygen. Our hypothesis is that automated oxygen therapy leads to a diminution on the length of hospital stay.

NCT ID: NCT03185533 Completed - Length of Stay Clinical Trials

Reducing Length of Stay in the Emergency Department

Start date: January 1, 2015
Phase: N/A
Study type: Observational

Emergency department (ED) crowding has become an international challenge in the recent decades. Length of stay (LOS) is a useful marker to monitor ED crowding. Searching for the possible causes and reducing barriers may have the greatest impact on EDLOS. Therefore, the investigators assembled a multidisciplinary team for improvement of the ED process, to undergo assessments of ED patient flow with the spirit of lean-sigma methodologies. The objectives of this study were to evaluate a Lean-sigma-based initiative to lessen EDLOS.

NCT ID: NCT03151616 Completed - Aged Clinical Trials

Anticholinergic Risk Scale and Resource Use After Elective Noncardiac Surgery

Start date: April 1, 2003
Phase: N/A
Study type: Observational

This study investigates the association of preoperative anticholinergic medication exposure with healthcare resource utilization in a population-based sample of older patients enrolled in a universal pharmacare program

NCT ID: NCT03132831 Completed - Arthroplasty Clinical Trials

Influence of the Operative Day on the Average Duration of Stay in Primary Hip and Knee Replacements

JourOpDMS
Start date: September 1, 2018
Phase:
Study type: Observational

Reducing the length of stay (LOS) after primary arthroplasty is a relatively new target that arouses the attention of orthopedic surgeons in order to return home early through the fast recovery protocols but this goal is also wanted in public health for the sake of overall decline health spending in public costs.

NCT ID: NCT02890927 Completed - Clinical trials for Cardiovascular Diseases

Geriatric-CO-mAnagement for Cardiology Patients in the Hospital

G-COACH
Start date: September 2016
Phase: N/A
Study type: Interventional

The primary objective of the evaluation study is to determine if geriatric co-management is superior to standard of care in preventing functional decline in older patients admitted for acute heart disease or Transcatheter Aortic Valve Implementation (TAVI) to the cardiology units of the University Hospitals Leuven.

NCT ID: NCT02738762 Withdrawn - Clinical trials for Mechanical Ventilation

Glutamine Supplementation

Start date: November 15, 2017
Phase: N/A
Study type: Interventional

Earlier studies showed a benefit in survival when glutamine was given intravenously and these studies lead to recommendations that glutamine should be given to critically ill patients. The ESPEN guidelines recommend 0,2-0,4 g/kg/d intravenous glutamine added to standard parenteral nutrition . Until recently it was not possible to obtain a plasma glutamine level fast enough to consider the result for clinical decision making. With the availability of a Point of Care (POCT) measurement of plasma glutamine level a measurement can be performed short after the collection of blood. This offers the possibility to identify a patient with a low plasma glutamine level shortly after admission and use repeated measurements for evaluation of the response to supplementation of glutamine.

NCT ID: NCT02687412 Completed - Clinical trials for Postoperative Complications

Fast-track Surgery After Gynecological Oncology Surgery

Start date: November 21, 2016
Phase: N/A
Study type: Interventional

Fast-track surgery (FTS) pathway, also known as enhanced recovery after surgery (ERAS), FTS is a multidisciplinary approach aiming to accelerate recovery, reduce complications, minimize hospital stay without an increased readmission rate and reduce healthcare costs, all without compromising patient safety. It has been used successfully in non-malignant gynecological surgery, but it has been proven to be especially effective in elective colorectal surgery. However, no consensus guideline has been developed for gynecological oncology surgery although surgeons have attempted to introduce slightly modified FTS programmes for patients undergoing such surgery. NO randomised controlled trials for now. The advantages of fast-track most likely extend to gynecology, although so far have scarcely been reported. There is a existing research showed FTS in gynecological oncology provide early hospital discharge after gynaecological surgery meanwhile with high levels of patient satisfaction. The aim of this study is to identify patients following a FTS program who have been discharged earlier than anticipated after major gynaecological/gynaecological oncologic surgery and analyze the complication after surgery.