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Postoperative Complications clinical trials

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NCT ID: NCT03010280 Completed - Clinical trials for Postoperative Complications

Effect of Immunonutrition on Inflamatory Markers After Bariatric Surgery

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

A prospective randomized clinical trial of all the patients undergoing Roux - en-Y gastric bypass will be performed. Patients will be randomly assigned into 2 groups: those patients receiving a preoperative balanced energy high-protein formula (group 1) and those receiving preoperative Immunonutrition (group 2). Changes between groups in acute inflamatory markers, pain, postoperative septic complications and lenght of stay, among others will be investigated.

NCT ID: NCT03009929 Completed - Clinical trials for Postoperative Complications

Validation Study of ClassIntra®

ClassIntra®
Start date: February 15, 2017
Phase:
Study type: Observational

Whereas there are several validated systems for reporting postoperative complications, there are only a few and not prospectively validated systems for reporting intraoperative complications. The investigators developed a definition and CLASSification for Intraoperative Complications CLASSIC within a Delphi study involving international interdisciplinary experts. As both surgery and anaesthesia may be involved in complications in the perioperative period, all patient-related intraoperative complications occurring between skin incision and closure are considered in this reporting system. CLASSIC was updated to ClassIntra® v1·0, by encompassing five severity grades to align with the validated Clavien-Dindo Classification for grading postoperative complications. The aim of this international multicentre observational cohort study is to assess the validity and practicability of this newly derived and updated classification system ClassIntra® in patient undergoing an in-hospital surgical procedure. Providing an easy applicable and internationally validated classification system is a contribution to improve quality of health care and patient safety.

NCT ID: NCT02987985 Completed - Anesthesia Clinical Trials

Efficacy of Opioid-free Anesthesia in Reducing Postoperative Respiratory Depression in Children Undergoing Tonsillectomy

Start date: October 15, 2017
Phase: Phase 3
Study type: Interventional

The objective of this trial is to determine whether an opioid-free general anesthetic (OFA) technique utilizing ketamine, dexmedetomidine, lidocaine, and gabapentin can help reduce postoperative respiratory depression in the post-anesthesia care unit and ward in children with sleep-disordered breathing undergoing tonsillectomy when compared with traditional opioid-containing techniques. It is expected that this OFA regimen will have a measurable reduction on postoperative respiratory depression in children with sleep-disordered breathing.

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: NCT02962024 Completed - Clinical trials for Postoperative Complications

Does Local Morphine Add to Local Anesthetics in Serratus Anterior Plane Block Has a System Analgesic Effect?

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

the investigators aim is to investigate and explore the effect 10 mg morphine added to local anesthetics in serratus anterior plane block for post mastectomy pain management after modified radical mastectomy in patients with breast cancer with assessment of its serum level if it will be absorbed systemically or not?

NCT ID: NCT02961140 Not yet recruiting - Anesthesia Clinical Trials

Different Anesthetic Managements of Esophageal Resection and Reconstruction

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

Anesthetic management and fluid therapy is crucial in esophageal resection and reconstruction, which is associated with high incidence of postoperative morbidity and mortality. This study aims to investigate the effect of goal directed fluid management on the postoperative outcome of esophageal resection and reconstruction.

NCT ID: NCT02961075 Completed - Clinical trials for Postoperative Complications

Impact of Local Anesthesia on Postbronchoscopy Fever: a Randomised Controlled Study

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

Impact of Local Anesthesia on Postbronchoscopy Fever: a Randomised Controlled Study

NCT ID: NCT02957825 Terminated - Clinical trials for Complication, Postoperative

Surveillance of High-risk Early Postsurgical Patients for Real-time Detection of Complications

SHEPHERD
Start date: February 2, 2018
Phase: N/A
Study type: Interventional

The aim of this study is to test the hypothesis that continuous wireless monitoring on the postsurgical ward will improve patient outcome, measured as disability-free survival at three months after surgery. Further, the investigators hypothesize that this tight control regimen decreases length of hospital stay and treatment costs in patients with complications.