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Postoperative Complications clinical trials

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NCT ID: NCT02980770 Recruiting - Clinical trials for Obstructive Sleep Apnea

Postoperative Complications in Patients With Obesity Hypoventilation Syndrome

OHBE
Start date: November 2016
Phase: N/A
Study type: Observational

Obstructive sleep apnea (OSA) and Obesity-Hypoventilation Syndrome (OHS) are common conditions in obesity, which may influence the prognosis in patients undergoing surgery. There is a need for simple screening tools to identify such patients at high risk. The current multicenter observational study aims to investigate occurrence of OSA and OHS in obese individuals undergoing elective abdominal surgery and further address its impact on perioperative and postoperative complications.

NCT ID: NCT02976571 Recruiting - Clinical trials for Postoperative Complications

Local and Intraperitoneal Analgetics in Gynecologic Laparoscopy for Post Operative Pain Relief

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

A comparison between local and intraperitoneal analgetics to placebo, during laparoscopy, regarding post operative pain.

NCT ID: NCT02962219 Recruiting - Clinical trials for Oesophageal Adenocarcinoma

Exercise Prior to Oesophagectomy

ExPO
Start date: September 2016
Phase: N/A
Study type: Interventional

The purpose of this feasibility study is to determine whether a structured exercise programme prior to oesophagectomy has: acceptable adherence, is safe, and improves physiological measures of physical fitness above standard care.

NCT ID: NCT02938871 Recruiting - Liver Disease Clinical Trials

Effect of Synbiotic on Postoperative Complications After Liver Transplantation

Start date: March 2016
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the use of synbiotic in patients after liver transplantation and assess the effect of these agents on postoperative infections, antibiotic use, length of hospital stay, mortality and nutritional status.

NCT ID: NCT02921932 Recruiting - Clinical trials for Perioperative/Postoperative Complications

The Impact of Prehabilitation Bundle on Perioperative Outcome for Frail Elderly Patients Undergoing Major Abdominal Surgery

Start date: March 1, 2017
Phase: N/A
Study type: Interventional

This study aims to study the efficacy of a preoperative "bundle" of interventions, which consists of preoperative physiotherapy, nutritional support and cognitive exercises on elderly frail patients undergoing major abdominal surgery, and evaluating their outcomes. There will be two arms, intervention and control.

NCT ID: NCT02878668 Recruiting - Clinical trials for Post-operative Complication

The Value of Infectious Biomarkers for Prediction of Complication After Hepatopancreatobiliary Surgery

Start date: April 2016
Phase: N/A
Study type: Observational

Post operative complication after hepatopancreatobiliary surgery is high as 30-50%,which is the main reason for patient admitted to ICU. Several biomarkers have been shown to be useful in the early diagnosis of sepsis and systemic bacterial infection. The purpose of this study is to assess the predictive value of biomarkers for early complication after hepatopancreatobiliary surgery and assess the effectiveness of anti-infectious therapy.

NCT ID: NCT02876406 Recruiting - Clinical trials for Postoperative Complications

ΔvapCO2 / Cav02 Ratio as a Prognostic Marker and Predictor of Complications After Cardiac Surgery

Start date: October 2016
Phase: N/A
Study type: Observational [Patient Registry]

This study evaluates the usefulness of the ΔvapCO2 / Cav02 ratio to predict complications after elective cardiac surgery, comparing it with others markers such as lactate, arteriovenous CO2 difference (ΔvapCO2) and would try to developed a new predictive score for postoperative complications.

NCT ID: NCT02829515 Recruiting - Clinical trials for Postoperative Complications

Tonsil Surgery in Sweden: A National Quality Register

NTSRS
Start date: May 2009
Phase:
Study type: Observational [Patient Registry]

For the purpose of quality assurance, the Swedish Association for Otorhinolaryngology and Head and Neck surgery has developed several national registers concerning ear, nose and throat care. One of these is the National Tonsil Surgery Registry in Sweden (NTSRS). In NTSRS patients undergoing tonsil surgery for benign indications are included. Data regarding indication, surgical methods and techniques as well as patient reported outcomes measures are collected. The register is designed to facilitate description of clinical activities in a unit and help identify the need of clinical improvement programs. By compiling national data, the register can be used to describe clinical practice in a large national cohort.

NCT ID: NCT02812199 Recruiting - Chronic Sinusitis Clinical Trials

Efficacy of Post-FESS Implantation of Composite Removable Sinus Stent to Prevent Post-Operative Complications

Start date: August 2016
Phase: N/A
Study type: Interventional

This is a randomized controlled first in man study. Study purpose is to assess safety and efficacy of Composite Removable Stent Composite Stent implantation post-endoscopic sinus surgery in terms of: - Sinus tissue adhesions - Middle turbinate lateralization into nasal septum i.e. postoperative opening reduction - Inflammation

NCT ID: NCT02776046 Recruiting - Clinical trials for Surgical Site Infection

Individualized Perioperative Open-lung Ventilatory Strategy With High Versus Conventional Inspiratory Oxygen Fraction (iPROVE-O2).

iPROVE-O2
Start date: June 1, 2017
Phase: N/A
Study type: Interventional

The iPROVE-O2 trial aims at comparing the efficacy of high and conventional FiO2 within a perioperative individualized ventilatory strategy to reduce the overall incidence of SSI.