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Surgery clinical trials

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NCT ID: NCT03468738 Completed - Surgery Clinical Trials

Investigation of the Transfusion Practices in Surgical Patients in Turkey

CeKATU
Start date: April 2, 2018
Phase:
Study type: Observational

The aim of this study is to describe the transfusion practices in patients undergoing major surgery in Turkey. The transfusion rates of red blood cells (RBC), fresh frozen plasma (FFP) and platelets; the transfusion predictors and transfusion related patient outcomes are investigated.

NCT ID: NCT03464981 Completed - Heart Failure Clinical Trials

Observational Hemodynamic Monitoring During LVAD Implantation Among Individuals With Advanced Heart Failure

BATMAN
Start date: September 10, 2018
Phase:
Study type: Observational

The overall objective of this pilot analysis is to characterize the hemodynamic changes that occur during implantation of a left ventricular assist device (LVAD) in patients with advanced heart failure - specifically, how right ventricular function is compromised as a result of LVAD implantation.

NCT ID: NCT03464721 Completed - Surgery Clinical Trials

Usability of SMART ANGEL Medical Device to Record and Transmit Health Data From Patient's Home Following Outpatient Surgery

SMART ANGEL 1
Start date: May 14, 2018
Phase:
Study type: Observational

This study represents the first step for testing this device in patients in real-life situations to evaluate the technological capacities and usability by the patient

NCT ID: NCT03462524 Completed - Surgery Clinical Trials

Neoadjuvant Therapy for Esophageal Cancer and Cardiopulmonary Physiology

Start date: January 1, 2010
Phase: N/A
Study type: Observational

Although recent global trends indicate reduced postoperative mortality after esophagectomy, major morbidity, in particular pulmonary, remains high, with considerable health and economic costs. In a recent modern international collaborative series of 2704 patients from high-volume centers, with an approximate equal mix of open and minimally invasive approaches, respiratory complications were evident in 28% of patients, pneumonia in 15%, and respiratory failure in 7%.1 In other series, respiratory failure is reported in up to 15% of patients and is the most common cause of mortality. Prediction of risk and prevention of respiratory morbidity is therefore of considerable importance, and in this context baseline assessment of respiratory physiology compliments clinical assessment, history and enhanced recovery pathways representing key elements of current patient management. In this study, which will include all prospective patients with locally advanced esophageal cancer treated at a National Center, pulmonary function will be systematically measured before and after neoadjuvant therapy. The investigators seek to evaluate the incidence of radiation induced lung injury (RILI), as well as subclinical changes in pulmonary physiology that may be linked to postoperative complications, and quality-of-life in survivorship, and to compare cohorts who received radiation therapy or chemotherapy alone, preoperatively.

NCT ID: NCT03461341 Completed - Surgery Clinical Trials

European iNvestigation of SUrveillance After Resection for Esophageal Cancer

ENSURE
Start date: June 1, 2009
Phase:
Study type: Observational

The ENSURE study will comprise two phases. Phase 1: European multicenter survey of surveillance protocols after esophageal cancer surgery ENSURE questionnaire will be circulated to representatives from participating European countries. Phase 2: European multicenter retrospective observational study of the impact of postoperative surveillance protocols on oncologic outcome and HR-QL Phase 2 will constitute a retrospective observational study of patients undergoing treatment with curative intent for esophageal cancer at participating Centers from June 2009 to June 2015.

NCT ID: NCT03446950 Completed - Surgery Clinical Trials

Study Investigating Role of Unalike Patient Positioning on PROMIS Scores

STIRUPPS
Start date: March 6, 2018
Phase: N/A
Study type: Interventional

The primary objective is to assess the impact of patient positioning using the candy cane stirrups as compared to boot stirrups on physical functioning outcomes at 6 weeks post-op

NCT ID: NCT03439631 Completed - Surgery Clinical Trials

Patient Satisfaction With Tiered OR Versus Status Quo OR

Start date: February 28, 2018
Phase: N/A
Study type: Interventional

Operating room (OR) costs consume a significant portion of hospital budgets. Standard or "Status Quo" ORs are equipped with the same, fixed set of assigned resources, regardless of case complexity or actual resource requirements. Allocation of resources in standard ORs is the same whether the participant is having heart surgery or bunion removal. The investigators propose a strategy for OR design and set up wherein resources are carefully matched to procedure complexity as a novel means of healthcare delivery. This prospective, comparative cohort pilot study will compare two operating room (OR) setup designs. The Tiered OR setup (study intervention) will be an efficiently staffed and equipped OR, geared to the complexity of the surgical procedure. The level of care provided would be equivalent to that of an out-patient day surgery setup. The Status Quo OR setup (control intervention) will be a standard fully equipped, fully staffed OR.

NCT ID: NCT03432429 Completed - Breast Cancer Clinical Trials

Real Time Tissue Characterisation Using Mass Spectrometry REI-EXCISE iKnife Study

REI-EXCISE
Start date: September 5, 2017
Phase:
Study type: Observational

REI-EXCISE is a multicentre, prospective, non-randomised feasibility study, aimed to evaluate the diagnostic accuracy of rapid ionisation mass spectroscopy using an iKnife device. The iKnife will collect vapour, a by-product of surgery, which will pass through the mass spectrometer machine for analysis in order to evaluate what is "normal" and what is "cancerous" breast tissue.

NCT ID: NCT03427294 Completed - Surgery Clinical Trials

Delphi Study on Rehabilitation Following Lumbar Arthrodesis

Start date: January 3, 2018
Phase:
Study type: Observational [Patient Registry]

Delphi study on perioperative rehabilitation after single and double level lumbar arthrodesis.

NCT ID: NCT03427281 Completed - Surgery Clinical Trials

Postoperative Bracing Patterns After Lumbar Surgery

Start date: January 10, 2018
Phase: N/A
Study type: Interventional

A variety of postoperative bracing are routinely applied after spinal procedures but there are limited data regarding their efficacy, especially with the increasing use of internal fixation.Currently, no data are available regarding the use of postoperative braces in Belgium. Bracing is sometimes considered after lumbar surgery for degenerative conditions. All neurosurgeons and orthopedical surgeons in Belgium will be questioned to assess the patterns of postoperative bracing use after lumbar surgery.