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Surgery--Complications clinical trials

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NCT ID: NCT05155878 Recruiting - Surgery Clinical Trials

Prognostic Factors in Periampullary Tumors and Cysts

Start date: September 1, 2021
Phase:
Study type: Observational [Patient Registry]

The project aims at analysing prognostic and predictive factors involved in diagnostics and surgical treatment of cysts and tumors in the pancreas and periampullary region using both clinical data and blood and tissue samples for biomarker development and validation.

NCT ID: NCT04973397 Recruiting - Clinical trials for Myocardial Infarction

Vascular Events In Patients Undergoing Same-day Noncardiac Surgery (VALIANCE) Study

VALIANCE
Start date: November 17, 2021
Phase:
Study type: Observational

The proportion of noncardiac surgeries performed as same-day surgery is increasing worldwide, with more complex surgeries being performed on higher risk patients in the outpatient setting. Little is known on the risk factors, incidence and prognosis of patients undergoing same-day noncardiac surgery. The main objective of this study is to inform on the incidence and risk factors of cardiovascular and other adverse events after same-day surgery and to develop risk prediction tools to better inform on the risk and selection of patients undergoing same-day surgery.

NCT ID: NCT04967391 Recruiting - Clinical trials for Head and Neck Cancer

Tumescence in HNC Skin Graft Reconstruction

Start date: September 1, 2021
Phase: Phase 3
Study type: Interventional

Our primary objective is to determine if the use of tumescence has a meaningful effect on STSG uptake at the recipient site. This is an important outcome because poor graft uptake results in the need for prolonged local wound care, additional clinic visits for patients and increased risk of infection. A prospective, randomized comparison of the tumescence to our current standard of care will allow us to definitively evaluate any benefits to this technique. Tumescence is commonly used in the treatment of burn patients to minimize blood loss during both tangential excision of eschar and during harvest of split-thickness grafts for reconstruction. This is considered the standard of care in burn surgery as using tumescence has been clearly demonstrated to reduce intraoperative blood loss during harvest of large skin grafts and excision of large burns when compared with the application of topical epinephrine as was the historic standard practice.4-6 Tumescence also creates a firm and uniform surface from which to harvest the skin graft, which the investigators believe may improve the quality of harvest and rate of skin graft take.

NCT ID: NCT04887415 Recruiting - Clinical trials for Cardiovascular Diseases

Respiratory Strength Training in Cardiac Surgical Patients

Start date: September 2, 2021
Phase: N/A
Study type: Interventional

Swallowing difficulty (dysphagia) is a common postoperative complication in patients who undergo cardiac surgical procedures. Postoperative dysphagia in cardiac surgical patients is associated with negative health-related outcomes including increased rates of pneumonia, reintubation, and death as well as increased length of hospital stay and costs of care. This study will examine the safety, feasibility, and impact of preoperative respiratory strength training (RST) on swallowing and associated health-related outcomes in cardiac surgical patients. We hypothesize that preoperative RST will be safe, well-tolerated, and lead to improved swallowing and health-related outcomes in cardiac surgical patients.

NCT ID: NCT04884841 Recruiting - Clinical trials for Surgery--Complications

Development and Validation of Models to Predict Postoperative Complications for Patients With Cardiac Surgery

DV_model_CS
Start date: January 1, 2012
Phase:
Study type: Observational

Patients undergoing cardiac surgery is routinely performed in clinical scenarios, highly postoperative morbidities and long-term mortality should be modified. A simple risk prediction model incorporating risk factors can help guide clinical decision making, patient counseling and treatment planning.

NCT ID: NCT04877535 Recruiting - Clinical trials for Surgery--Complications

Pilot Study for Postoperative Machine Learning

Start date: June 3, 2021
Phase: N/A
Study type: Interventional

The objectives of the study are to determine the interpretability, workflow role, and effect on communications of showing report cards containing Machine Learning (ML)-based risk profiles based on pre- and intra-operative data to postoperative providers.

NCT ID: NCT04824066 Recruiting - Clinical trials for Surgery--Complications

The Role of Wearable Devices in Cardiothoracic Surgery: Predicting and Detecting Early Postoperative Complications

Start date: July 10, 2021
Phase:
Study type: Observational

The overarching goal of this research is to use machine learning analysis of high-resolution data-collected by wearable technology-of cardiothoracic surgical patients to assess recovery and detect complications at their earliest stage

NCT ID: NCT04796740 Recruiting - Thrombosis Clinical Trials

Thrombembolism After Robot- Assisted Surgery in Urology

Start date: December 17, 2019
Phase:
Study type: Observational

Cancer patients have an increased risk of perioperative complications undergoing surgery procedures. Postoperative complications caused by thrombembolic events after robot- assisted surgery in major urological procedures have been reported and associated with an increased lenght of stay in the hospital. We therefore aimed to investigate in a retrospective analysis 250 patients undergoing robotic-assisted radical cystectomy and prostatectomy procedures for risk factors for thrombembolic events in this specific patient population.

NCT ID: NCT04732403 Recruiting - Clinical trials for Surgery--Complications

Ureteral Jets and Patient Positioning Study

Start date: February 1, 2021
Phase: N/A
Study type: Interventional

The objective of the study is to identify the relationship between patient position during surgery and time to confirmation of ureteral patency on cystoscopy.

NCT ID: NCT04725305 Recruiting - Postoperative Pain Clinical Trials

BiZact Tonsillectomy in the Pediatric Population

Start date: June 6, 2021
Phase: N/A
Study type: Interventional

This study has been designed to evaluate how effective the Bizact tonsillectomy device is in reducing operating time and complications that occur after surgery. This device operates in a different way than the standard device that is used for most tonsillectomies. In 2019, a study was conducted in 186 children and adults using this device in tonsillectomies. Results showed lower blood loss and shortened time in surgery. However, the rate for bleeding as a complication after surgery was the same as other procedures that are used in tonsillectomy