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Postoperative Complications clinical trials

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NCT ID: NCT03922737 Enrolling by invitation - Clinical trials for Post-Op Complication

Telehealth Following Orthopaedic Procedures

Start date: October 6, 2017
Phase: N/A
Study type: Interventional

This study aims to evaluate the quality of care provided by a home-based teleheath program as a safe and acceptable alternative to an in-person office visit as determined by satisfaction with the program and the amount of further medical management required by the patients.

NCT ID: NCT03234543 Enrolling by invitation - Liver Diseases Clinical Trials

Remote Ischemic Conditioning in Abdominal Surgery

Start date: October 8, 2017
Phase: N/A
Study type: Interventional

This phase II randomized (1:1) controlled trial will examine the effects of remote ischemic conditioning (RIC) on the outcomes of major abdominal surgery. One hundred subjects will be enrolled at a single institution - University Hospital - Newark. The study population are patients undergoing major abdominal surgery (anticipated to be >/= 2 hrs long with a hospital stay >/= 2 days). Subjects in the treatment group will receive lower limb ischemic conditioning at 3 different time points: before surgery, POD 1 and POD 2. The primary outcome is the 30-day comprehensive complications index (CCI). Key secondary outcomes are changes in systemic inflammatory markers in peripheral blood and 30-day mortality.

NCT ID: NCT02939664 Enrolling by invitation - Weight Loss Clinical Trials

Laparoscopic Gastric Bypass Versus Laparoscopic Banded Gastric Bypass Randomized Prospective Clinical Trial

LGB-vs-LbGB
Start date: April 2016
Phase: N/A
Study type: Interventional

This study try to identify differences in length of operation, weight loss and complications, between two different bariatric surgical techniques, the laparoscopic Roux-en-Y gastric bypass and the laparoscopic Roux-en-Y banded gastric bypass. The study will be conducted in a Spanish public health system hospital. The patients of the trial will have the preoperative studies, hospital treatment during the admission, postoperative treatment and follow up as any other patient included in the hospital bariatric surgery program. The study cases will have placed around the gastric pouch a band of polypropylene mesh, and will be randomly choose between the participants. Patients will be randomized in a 5/3 (study/control) ratio.

NCT ID: NCT02572531 Enrolling by invitation - Clinical trials for Postoperative Complications

Effect of Probiotics on Pain and Oral Wound Healing After Third Molar Surgery

PROVIS
Start date: September 1, 2016
Phase: N/A
Study type: Interventional

The aim of this research is to study the effect of probiotic supplements (Lactobacillus reuteri) on post-surgical complications and oral wound healing after extraction of impacted third molars.

NCT ID: NCT02084615 Enrolling by invitation - Clinical trials for Postoperative Complications

Prospective Study Investigating Aspirin and Intraoperative Blood Loss and Complications Following Inguinal Hernia Repair

Start date: August 2014
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether aspirin taken in the perioperative period will increase the blood loss associated with open inguinal hernia repairs. A secondary purpose of this study is to determine if the aspirin administered in the perioperative period increases the risk of complications associated with open inguinal hernia repairs.

NCT ID: NCT01744938 Enrolling by invitation - Clinical trials for Postoperative Complications

Preoperative Biliary Drainage for the Lower Malignant Obstructive Jaundice

Start date: September 2012
Phase: Phase 3
Study type: Interventional

Patients with the lower malignant obstructive jaundice planned to do the pancreaticoduodenectomy, receiving preoperative biliary drainage or early surgery (without preoperative biliary drainage), both groups has the similar surgical morbidity, no statistics significance.

NCT ID: NCT00606372 Enrolling by invitation - Clinical trials for Ischemic Heart Disease

On-Pump vs. Off-Pump CABG in High-Risk Patients (EuroSCORE 6+)

PRAGUE 6+
Start date: June 2006
Phase: N/A
Study type: Observational

Previous studies comparing on-pump and off-pump operating strategy did only partially demonstrate benefits of the off-pump myocardial revascularisation.In primary end-points (MI, death, renal failure, and so on) there was no significant difference, but in secondary end-points we observed benefits resulting for patients. We would like to show the benefit of the method without extracorporeal circulation in patients with higher and hight operation risk, coming from EuroSCORE classification system (6 points and more).