Clinical Trials Logo

Postoperative Complications clinical trials

View clinical trials related to Postoperative Complications.

Filter by:

NCT ID: NCT01460615 Completed - Clinical trials for Postoperative Complications

Cortisone Treatment for the Prevention of Postoperative Pancreatitis and Pancreatitis-induced Complications After Pancreaticoduodenectomy and Distal Pancreatic Resection

Start date: February 2011
Phase: Phase 2
Study type: Interventional

The purpose of this randomized, placebo-controlled trial is to investigate whether postoperative pancreatitis and other immediate complications after pancreaticoduodenectomy or distal pancreatic resection may be reduced with cortisone treatment. Treatment is administered to high risk patients (defined by high amount of acinar cells in the cut edge of pancreas).

NCT ID: NCT01458678 Completed - Clinical trials for Postoperative Complications

Non Invasive Methods to Guide Volume Optimization

Start date: November 2011
Phase: N/A
Study type: Interventional

Goal directed volume therapy means that bolus doses of 150-250 ml colloid fluid is administered to the patient during contemporary measurement of the patients stroke volume. The fluid status is considered optimized when stroke volume no longer increases with more than 10%, indicating that the patient is close to the top of the Frank-Starling curve. Several studies show that volume optimization reduces hospital stay and reduces the amount of surgical complications. The overall purpose is to investigate if the much more simple non invasive technique Pleth Variability Index can replace oesophageal doppler to guide volume therapy in routine health care, and to analyse if a volume kinetic test can be used to evaluate hypovolemia before surgery and make specific rehydration possible by analysing the correlation between this test and fluid optimization using stroke volume measurements. Primary hypothesis: 1. The volume of colloids that is given to volume optimise an anesthetized patient using Pleth Variability Index shows a good correlation to the volume used if volume optimisation is undertaken by the guidance of oesophageal doppler. 2. Data from the two methods correlate and discriminates similarly volume responders from non responders. 3. A volume kinetic model that indicates dehydration can predict the need for rehydration in order to achieve a well hydrated patient at start of surgery.

NCT ID: NCT01450631 Completed - Clinical trials for Surgical Site Infection

The Use of the Prevena™ Incision Management System on Post-Surgical Cesarean Section Incisions

Start date: February 2012
Phase: N/A
Study type: Interventional

The purpose of this study is to compare the post-surgical standard-of-care dressing to the Prevena™ Incision Management System in women undergoing Cesarean section surgery.

NCT ID: NCT01445990 Completed - Clinical trials for Postoperative Complications

Efficacy Study of Free Flap Monitoring Using Capillary Lactate and Glucose Measurements

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

Evaluation of capillary glycaemia and lactataemia measurements for pedicle impairments diagnosis in free tissue transfers is realized. These measures are done after surgical reconstructions with free tissue flap, simultaneously with clinical examination. These biological data aren't available to make clinical diagnosis of complication; only clinical examination is allowed in this way. A posteriori, clinical and biological parameters will be compared in order to determine if capillary glycaemia and lactataemia measurements is a good procedure for free tissue flaps monitoring.

NCT ID: NCT01423136 Completed - Clinical trials for Postoperative Complications

Remote Electrocardiographic (ECG) ST-Monitoring (PROSE 3)in Post-op Patients

PROSE 3
Start date: October 2010
Phase: N/A
Study type: Observational

In moderate to high risk patients, cardiovascular complications after surgery account for almost 60% of death after surgery. This study will randomize 140 patients into routine postop care with Holter monitoring versus routine postop care + remote ST monitoring + Holter monitoring. The response time to electrocardiographic (ECG) ST changes as well as the total ischemia time will be studied.

NCT ID: NCT01418807 Completed - Postoperative Pain Clinical Trials

Transumbilical Versus Transvaginal Specimen Retrieval at Minilaparoscopy

Start date: July 2011
Phase: Phase 2/Phase 3
Study type: Interventional

We hypothesise that pain at minilaparoscopy for gynecologic disease is reduced when transvaginal rather than transumbilical specimen extraction is accomplished. This would be due to the avoidance of a 10-mm port in the umbilicus. Visual analogue scale score of post-operative pain will be obtained and patients satisfaction will be asked at the 2-month postoperative visit.

NCT ID: NCT01416077 Completed - Esophageal Cancer Clinical Trials

Decreasing Postoperative Complications by Goal-Directed Fluid Therapy During Esophageal Resection

Start date: October 2011
Phase: Phase 4
Study type: Interventional

Surgery for cancer of the esophagus is associated with a high risk of postoperative complications. It has been shown that the risk of postoperative complications can be decreased by optimising the amount and type of infusion fluids given during surgery, steered by measurement of cardiac stroke volume, mostly done with a device called esophageal Doppler. This device can however not be used during this type of surgery. This study wants to test the hypothesis that postoperative complications in patients operated for esophageal cancer can be partially prevented by using a goal directed strategy for the administration of fluids and drugs influencing the heart and vessels, based on measurement of stroke volume by pulse wave analysis (FloTrac).

NCT ID: NCT01406769 Completed - Lymphedema Clinical Trials

Bioimpedance Spectroscopy in Detecting Lower-Extremity Lymphedema in Patients With Stage I, Stage II, Stage III, or Stage IV Vulvar Cancer Undergoing Surgery and Lymphadenectomy

Start date: July 16, 2012
Phase: Phase 2
Study type: Interventional

This phase II trial studies bioimpedance spectroscopy in detecting lower-extremity lymphedema in patients with stage I, stage II, stage III, or stage IV vulvar cancer undergoing surgery and lymphadenectomy. Diagnostic procedures, such as bioimpedance spectroscopy, may help doctors to predict the onset of lower-extremity lymphedema in patients with vulvar cancer undergoing surgery.

NCT ID: NCT01403961 Completed - Clinical trials for Postoperative Complications

Hemoglobin A1c and Immediate Postsurgical Complications Diabetes Type 2

HbA1c
Start date: July 2011
Phase:
Study type: Observational

The purpose of this study is to evaluate Hemoglobin A1c values previous to a surgery in patients with diabetes type II and the complication incidence in immediate post surgery.

NCT ID: NCT01391988 Completed - Clinical trials for Complication, Postoperative

Trial Comparing Electric and Harmonic Scalpel in Mastectomy

Harmonic
Start date: January 2008
Phase: Phase 3
Study type: Interventional

Prospective trial comparing post-operative complications and seroma formation after mastectomy in patients with breast cancer, using conventional electric scalpel and harmonic scalpel.