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Postoperative Complications clinical trials

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NCT ID: NCT02337010 Completed - Clinical trials for Postoperative Complications

Continuous Central Venous Oxygen Saturation Assisted Intraoperative Hemodynamic Management

Start date: October 2010
Phase: N/A
Study type: Interventional

Patients who are scheduled for: elective oesophageal tumour resection, total gastrectomy, pancreas resection, major vascular, total cystectomy will be recruited.To investigate effects of central venous pressure (CVP) and central venous saturation (ScvO2) guided fluid management on intraoperative haemodynamic parameters, volume and vasopressor requirement, and postoperative organ function and postoperative inflammatory response.

NCT ID: NCT02333747 Completed - Clinical trials for Postoperative Complications

Can Transcutaneous Electrical Acupoint Stimulation Improve the Quality of Recovery After Thyroidectomy?

Start date: January 2015
Phase: N/A
Study type: Interventional

The effect of transcutaneous electric acupoint stimulation (TEAS) on the quality of recovery in patients undergoing thyroidectomy surgery remains unclear. Therefore, the investigators conducted this prospective, randomized, double-blind study to verify the hypothesis that pre-operative TEAS could improve the quality of recovery (QoR) after thyroidectomy surgery.

NCT ID: NCT02323984 Completed - Clinical trials for Postoperative Complications

Postoperative Delirium in Hip Arthroplasty Patients

mRNAOrtho
Start date: January 2014
Phase: N/A
Study type: Observational

Identification of specific circulating microRNAs and microemboli formation (diagnosed by TC Doppler) in both delirious groups and nondelirious group will be our primary target. Delirium assessment through standardized questionnaires will be done at baseline (day of the surgery - pre operatory), immediately after surgery (in post anesthesia care unit) and then every 12 hours in Day 1 and Day2 after surgery. The investigators will use linear mixed models to describe the change patterns overtime, and compare differences at each time point. Inflammatory biomarkers will be explored overtime as well. The investigators will also explore age effect on cognitive function - cognitive reserve - based on the score of the cognitive test administered at baseline.

NCT ID: NCT02322567 Completed - Clinical trials for Kidney Transplantation

Left Ventricular Diastolic Dysfunction in Kidney Recipients

Start date: January 2012
Phase: N/A
Study type: Observational

The purpose of this study is to examine the relationship between pre-operative LV diastolic function and post-operative complications and kidney function in living-donor kidney transplantation patients.

NCT ID: NCT02313519 Completed - Clinical trials for Postoperative Complications

Probiotics in the Prevention of Complications After Colorectal Surgery

Start date: April 2013
Phase: Phase 4
Study type: Interventional

Based on the need of large-scale, trials to explore the use of probiotics to reduce post-operative complication rate, a randomized controlled trial is designed to investigate the impact of a probiotics treatment protocol on postoperative morbidity in an open elective colonic surgery cohort. The major objective is reduction of post-operative complications after 30 days.

NCT ID: NCT02309944 Completed - Obesity Clinical Trials

Negative Pressure Wound Therapy in Obese Gynecologic Oncology Patients

Start date: May 2015
Phase: N/A
Study type: Interventional

The purpose of the study is to test whether the use of a new wound closure technique can decrease the rates of wound complications in obese cancer patients.

NCT ID: NCT02267538 Completed - Delirium Clinical Trials

Dexmedetomidine and Delirium in Patients After Cardiac Surgery

Start date: November 2014
Phase: Phase 4
Study type: Interventional

Postoperative delirium (POD) is a frequently occurring complication after cardiac surgery. Its occurrence is associated with worse outcomes of patients, including increased morbidity, prolonged hospital stay, increased medical cost, and higher mortality. It is also associated with long-term cognitive decline and decreased quality of life. However, until recently, pharmacological interventions that can effectively prevent its occurrence are still limited. The purpose of this study is to investigate whether perioperative dexmedetomidine use can decrease the incidence of postoperative delirium in patients undergoing cardiac surgery.

NCT ID: NCT02265991 Completed - Clinical trials for Postoperative Complications

Prospective Biomechanical Analysis of Donor-site Morbidity Following Microvascular Fibula Transplantation

Start date: September 2011
Phase: N/A
Study type: Observational

Pre- and postoperatively patients who underwent free fibula flap were examined regarding donor-site morbidity of the lower extremities.

NCT ID: NCT02250898 Completed - Pain Clinical Trials

Massage for Post Breast Surgery

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

The aims of this study are to determine the effectiveness of myofascial massage specific to the breast/chest/shoulder area in reducing self-reported pain and increasing mobility among patients who have undergone a mastectomy or other breast surgery compared to a control group receiving global relaxation massages.

NCT ID: NCT02239159 Completed - Surgery Clinical Trials

Acupuncture-assisted-anesthesia to Improve Postoperative Outcome After Digestive Surgery in Elderly Patients

AID
Start date: April 2014
Phase: N/A
Study type: Interventional

The investigators assume that transcutaneous electric acupoint stimulation (TEAS) pretreatment may activate the endogenous protective mechanism, as a result protect the patients against subsequent surgical stress pregnancy. And TEAS may induce the production of endogenous analgesic transmitters, so develop an anesthetic-sparing effect. The investigators believe this intervention will reduce the subsequent incidence, duration and severity of organ dysfunction, possibly reducing the morbidity, even mortality. So in this study, the investigators hypothesize that TEAS before anesthesia and during surgery would decrease the morbidity and mortality of postoperative complications in 30 days after digestive surgery in elderly patients .