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Postoperative Complications clinical trials

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NCT ID: NCT04333693 Not yet recruiting - COVID-19 Clinical Trials

Outcomes of Vascular Surgery in COVID-19 Infection: National Cohort Study

Covid-VAS
Start date: April 1, 2020
Phase:
Study type: Observational [Patient Registry]

There is an urgent need to understand the outcomes of COVID-19 infected patients who undergo surgery, specially vascular surgery. Capturing real-world data and sharing Spanish national experience will inform the management of this complex group of patients who undergo surgery throughout the COVID-19 pandemic, improving their clinical care. The global community has recognised that rapid dissemination and completion of studies in COVID-19 infected patients is a high priority, so we encourage all stakeholders (local investigators, ethics committees, IRBs) to work as quickly as possible to approve this project. This investigator-led, non-commercial, non-interventional study is extremely low risk, or even zero risk. This study does not collect any patient identifiable information (including no dates) and data will not be analysed at hospital-level.

NCT ID: NCT04326088 Completed - Clinical trials for Head and Neck Cancer

Postoperative Complication After Free Flap Reconstruction for Head and Neck Cancer

Start date: April 1, 2018
Phase:
Study type: Observational

This study was designed to investigate the outcome of free-flap reconstruction surgery following head and neck cancer resection between primary and recurrent head and neck cancer patients.

NCT ID: NCT04307654 Completed - Clinical trials for Lactacidemia and Complications

Lactate and Complications in Cytoreduction Surgery for Peritoneal Carcinomatosis

Start date: January 2014
Phase:
Study type: Observational

Serum lactate is a risk factor for postoperative complications in patients undergoing cytoreduction surgery in peritoneal carcinomatosis

NCT ID: NCT04306562 Terminated - Cancer Clinical Trials

Effect of Oral Protein Supplementation on Postoperative Complications in Elderly Sarcopenic Cancerous Patients

Start date: October 1, 2019
Phase: N/A
Study type: Interventional

Sarcopenia is a condition of reduced skeletal muscle associated with aging. It leads to poor outcome and increased risk of postoperative complications. Achieving protein and energy requirements is crucial point in sarcopenia treatment. In preoperative patients, daily consumption of protein should be at least 1.2-2.0 g of protein/kg/day or 25-35 g of protein in a meal to provide muscular protein synthesis. The objective of this study is to show that preoperative enteral protein supplementation in elderly cancerous patients, who are diagnosed with sarcopenia, can decrease morbidity such as postoperative complications; mortality and improve postoperative clinical outcomes after elective surgery.

NCT ID: NCT04306133 Completed - Pain Clinical Trials

PENG Block Combined to Wound Infiltration for Hip Replacement

Start date: March 9, 2020
Phase: N/A
Study type: Interventional

This study analyze the effect of Pericapsular Nerve Group (PENG) Block combined to wound infiltration for analgesia after elective hip replacement. Half of participants will receive a PENG Block combined with wound infiltration, while the other half will receive wound infiltration alone.

NCT ID: NCT04304573 Not yet recruiting - Clinical trials for Postoperative Complications

Is Correcting Total Serum Calcium Levels Important After Thyroidectomy

Start date: June 9, 2020
Phase:
Study type: Observational

This study is designed as a prospective non-randomized longitudinal single- center cohort study to evaluate the importance of correcting total serum calcium levels. It will enroll around 100 patients undergoing total thyroidectomy with data being collected from March 2020 up to August 2020. The aim of this study is to determine whether total serum calcium level should be corrected for serum albumin in assessing symptomatic hypocalcemia after total thyroidectomy and which variable (total serum calcium, ionized calcium, corrected serum calcium for albumin with Payne's formula or early PTH) is the most valuable predictor of symptomatic hypocalcemia after total thyroidectomy.

NCT ID: NCT04302142 Withdrawn - Clinical trials for Intubation Complication

Effect of Applying Cuff Air Leak Pressure as Intraoperative Cuff Pressure on Postoperative Complications

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

The purpose of the study is to achieve effective ventilation with critical intracuff pressure (Pcr) and determine if application of Pcr reduces the risks associated with over-insufflation of endotracheal cuff including postoperative sore throat, cough,nausea, vomiting, aspiration, and pneumonia.

NCT ID: NCT04301232 Completed - Clinical trials for Post-Op Complication

Fast-Track Eligibility and Hospital Discharge for Outpatient Lumbar Discectomy

Start date: May 10, 2018
Phase:
Study type: Observational [Patient Registry]

122 ASA I-II patients were enrolled into the study. IV propofol, fentanyl and rocuronium were used for the induction and a total intravenous anesthesia technique for the maintenance of anesthesia. Sugammadex was given for neuromuscular blockade reversal. A multi-modal analgesic regimen was utilized. Primary outcome measures were PACU bypass rates and hospital discharge times. Secondary outcome measure was to compare discharge scoring systems for PACU bypass assessment: modified Aldrete Scoring System (mASS), White's Fast-Tracking Scoring System (WFTSS), and SPEEDS criteria

NCT ID: NCT04294797 Completed - Clinical trials for Postoperative Complications

Presepsin as a Predictor for Postoperative Complications Following Pancreatic Resection

Start date: July 11, 2017
Phase: N/A
Study type: Interventional

The study investigates the local and systemic inflammatory response following pancreatic resections.

NCT ID: NCT04293653 Active, not recruiting - Frailty Clinical Trials

Protocol for Patients Above 75 Years Undergoing Emergency Laparotomy

(ProPEL)
Start date: January 21, 2020
Phase: N/A
Study type: Interventional

In the ProPEL study the effect of a protocol designed for elderly patients about to undergo emergency abdominal surgery will be investigated. The protocol addresses issues of both frailty and ceiling-of -care decisions.