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NCT ID: NCT03185403 Completed - Oesophageal Cancer Clinical Trials

The Hemodynamic Effect Between Two Types of Anesthesia in Esophageal Surgery

HEMOBLOC
Start date: December 2013
Phase: N/A
Study type: Interventional

Continuous Paravertebral block (PVB) was reported to provide less episodes of hypotension than continuous thoracic epidural block (TEB). The maintenance of optimal tissue perfusion is essential for esophageal anastomosis in patients undergoing oesophagectomy. the aim of this study is to compare Hemodynamic effect of continous PVB compared to TEB , in patient undergoing oesophagectomy with laparoscopy and thoracotomy.

NCT ID: NCT03185052 Completed - Clinical trials for Peripheral Arterial Disease

Feasibility of Outpatient Care After Manual Compression in Patients Treated for Peripheral Arterial Disease by Endovascular Technique With 5F Sheath Femoral Approach

FREEDOM OP
Start date: September 27, 2017
Phase: N/A
Study type: Interventional

Over the past years, arterial closure systems have tended to replace manual compression to ensure hemostasis at femoral artery puncture points. Arterial closure systems reduce hemostasis and patient immobilization times, thus enabling early resumption of walking. These devices have contributed extensively to the development of outpatient stays for cardiology, vascular and neuro-radiology procedures. According to certain studies however, it would appear that arterial closure devices do not present any greater benefits than manual compression in terms of hemostasis and complications. Moreover, the use of increasingly small diameter instruments would tend to render manual compression sufficient. Finally, the use of these devices generates additional costs. The purpose of our prospective study is to evaluate the feasibility and safety of same-day discharge after manual compression in patients treated for peripheral artery disease by endovascular technique with 5F sheath.

NCT ID: NCT03184207 Completed - Intubation Clinical Trials

A Systematic Echography During Intubation Procedure to Predict Cardiovascular Collapse

EPIC
Start date: June 21, 2017
Phase:
Study type: Observational

In the operating room, most intubation procedures (IP) are scheduled and performed on hemodynamically stable patients. In the ICU, IP is frequently performed in emergent patients, because of unstable hemodynamics and/or acute respiratory failure, and complicated by a subsequent cardiovascular collapse. Transthoracic echocardiography (TTE) has become readily available in most ICUs for several years. Echocardiography enables to perform a noninvasive hemodynamic evaluation (cardiac function and volemia status). We hypothesized that performing a TTE prior to IP may help to predict cardiovascular collapse and its components.

NCT ID: NCT03184051 Completed - Knee Osteoarthritis Clinical Trials

Diagnostic Performance of Ultrasound Imaging Technique for Femoral Condyle Cartilage Evaluation and Osteoarthritis

CARTILAGE
Start date: June 15, 2017
Phase:
Study type: Observational

This study investigates the potential of the ultrasound imaging technique to diagnose the severity of knee osteoarthritis (OA). In parallel, measurements will also be conducted using Magnetic Resonance Imaging (MRI) and histology analysis as reference tools.

NCT ID: NCT03182387 Completed - Coma Clinical Trials

Key to Improve DiagNosis in Aspiration Pneumonia

KIDNAP
Start date: August 21, 2017
Phase:
Study type: Observational

To evaluate the diagnostic performance of amylase assay performed from bronchial alveolar fluid to differentiate aseptic chemical inhalation pneumonitis from an infectious inhalation pneumonitis in comatose patients with intubated ventilation for less than 24 hours.

NCT ID: NCT03182166 Completed - Ulcerative Colitis Clinical Trials

Golimumab in Ulcerative Colitis (UC) Patients With Loss of Response (LOR) Followed by Dose Optimization

GOLILOR
Start date: November 21, 2017
Phase: Phase 2
Study type: Interventional

It is planned to enroll 80 UC patients who will require optimization of golimumab after secondary LOR. The review of the study protocol and its approval by an Independent Ethics Committee of the University of Saint Etienne are pending. All patients enrolled will give their written informed consent before being included. This study will be conducted in accordance with the ethical principles that have their origins in the Declaration of Helsinki, in compliance with the approved protocol, good clinical practice and applicable regulatory requirements. Patients will visit the investigator from screening visit to visit 6 at W-1, W0, W2, W4, W8, and at the end of the follow-up at wk 24. During their participation, patients will record clinical parameters required to calculate the partial Mayo score reported over 3 days prior to the visit and endoscopy at W0, W2 (optional) , W4, W8 (optional) and at the end of the follow-up to calculate total Mayo score.

NCT ID: NCT03181802 Completed - Clinical trials for Chronic Low-back Pain

Are Paraspinous Intramuscular Injections of Botulinum Toxin A (BoNT-A) Efficient in the Treatment of Chronic Low-back Pain (LBP)?

BoNT-A
Start date: November 18, 2003
Phase: Phase 3
Study type: Interventional

Studying the therapeutic effect of paravertebral injections of BoNT-A (botulinum toxin A) requires further studies to confirm the reported short-term therapeutic effect and to determine potential predictive factors of efficacy.

NCT ID: NCT03181503 Completed - Prurigo Nodularis Clinical Trials

Safety and Efficacy of Nemolizumab in PN

Start date: October 2, 2017
Phase: Phase 2
Study type: Interventional

The aim of this study is to assess the safety and efficacy of nemolizumab in subjects with prurigo nodularis.

NCT ID: NCT03181425 Completed - Knee Osteoarthritis Clinical Trials

Magnetic Resonance Imaging Diffusion Tensor Tractography for Early Osteoarthritis Assessment

TRACTILAGE
Start date: October 2016
Phase: N/A
Study type: Observational

The aim of this study is the evaluation of new MRI tractography maps for early knee osteoarthritis assessment.

NCT ID: NCT03181412 Completed - Stroke Clinical Trials

Stroke Cincinnati Prehospital Stroke Severity Scale Evaluation iN prEhospital

SCENE
Start date: June 25, 2018
Phase:
Study type: Observational

The effectiveness of acute ischemic stroke (AIS) management has improved considerably in recent years with thrombolysis and more recently with mechanical thrombectomy (MT). Currently, mechanical thrombectomy can only be performed in stroke unit with an interventional neuroradiology center by experienced/qualified interventional neuroradiologists. In the Rhone area, only one hospital has the authorization to perform mechanical thrombectomy. Therefore, transferring directly eligible acute ischemic stroke patients for mechanical thrombectomy to this center constitutes an important stake of the triage of suspected acute ischemic stroke patients. Some validated scores for the identification of severe strokes and large vessel occlusion, including the Cincinnati prehospital stroke severity scale (CPSSS), appear to be relevant for pre-hospital use in order to identify patients potentially eligible for mechanical thrombectomy and address them to a stoke unit with interventional radiology center.