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Postoperative Complications clinical trials

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NCT ID: NCT01983176 Completed - Clinical trials for Postoperative Complications

Retrospective Clinical Outcome of Parotid Tumor Surgery

Start date: October 2013
Phase: N/A
Study type: Observational

The aim of this study was to determine the histopathological results of parotid tumors and postoperative complications after partial superficial or total parotidectomy with facial nerve dissection and superficial musculoaponeurotic system reconstruction.

NCT ID: NCT01959360 Completed - Hip Osteoarthritis Clinical Trials

Minimal Invasive Surgery in Total Hip Arthroplasty Patients; Strength, Functionality and Post Operative Complications

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

The aim of the present study is to explore the most efficient surgical approach in total hip replacement in short and long term when concerning strength, functionality and postoperative complications. The objective is to register muscular strength, hip joint functionality/mobilisation and complications after total hip arthroplasty (THA) performed by two minimal invasive/incision surgeries (MIS) versus the traditionally lateral approach. The primary working hypothesis is that due to a minimal dissection and reduced trauma in the muscles, patients will tolerate early hospital discharge better after MIS than after traditional lateral surgery. Patients in the MIS group will also be more active and maintain muscular strength and hip joint functionality/mobilisation better than patients in the lateral group.

NCT ID: NCT01927185 Completed - Clinical trials for Perioperative/Postoperative Complications

Long-versus Short-Axis Ultrasound Guidance for Subclavian Vein Cannulation

Start date: June 2013
Phase: N/A
Study type: Interventional

Central venous catheterization is commonly applied in patients undergoing cardiac surgery. The subclavian vein has lower risk of infection and provides more patients comfort. However central venous catheterization may results in complications such as pneumothorax, hemothorax or arterial puncture. It has been suggested that ultrasound (US) guidance could improve the success rate, reduce the number of needle passes and decrease complications. Two different real-time 2-dimensional US techniques can be employed in the insertion of central venous catheters. The first technique involves real-time US-guided cannulation of subclavian vein using a long axis/in-plane approach. The second one involves real-time US-guided using a short axis/out-off-plane approach. However to date no studies have compared their efficacy and safety. The purpose of this study was to compare the US-guided long-axis versus short-axis approach for the SCV catheterization in adult critical care patients.

NCT ID: NCT01921361 Completed - Clinical trials for Perioperative/Postoperative Complications

The Effects of Dexmedetomidine on Peroperative Shivering Incidence Under Spinal Anesthesia

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

The purpose of this study to compare the efficacy of intravenous or intrathecal dexmedetomidine on the incidence of shivering on patients who scheduled spinal anesthesia for elective surgery.

NCT ID: NCT01914328 Completed - Clinical trials for Postoperative Complications

Postoperative Pulmonary Complications in Major Abdominal Surgery

PPC
Start date: June 2013
Phase:
Study type: Observational

The purpose of this study is to determine the incidence of pulmonary complications in patients undergone major abdominal elective surgery performed under general anesthesia.

NCT ID: NCT01909700 Completed - Clinical trials for Post Operative Complications

Single Incision Pelvic Floor Mesh Implants

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

Objectives: To evaluate whether the use of single incision un-anchored small mesh implants is feasible, safe and effective for women with moderate pelvic organ prolapse. Design: Patients diagnosed with moderate pelvic organ prolapse were enrolled to undergo a single incision un-anchored mesh operation. Follow-up was 4 to 23 months. The outcome measures for this study were the operative safety and post-operative pain, adverse effects and anatomical as well as functional cure. Setting: The operations were performed under general anesthesia according with the reported surgical techniques at university and private hospitals.

NCT ID: NCT01907984 Completed - Clinical trials for Postoperative Complications

Diclofenac Administered Before Skull Operations Reduces the Severity of Headache After the Intervention

Start date: December 2012
Phase: Phase 4
Study type: Interventional

Purpose: According to the proposal of the International Headache Society acute postcraniotomy headache (PCH) is defined as a headache of variable intensity, being most serious at the site of surgical intervention and developing within 7 days after craniotomy. Typically, pain resolves within 3 months after surgery. According to the literature the incidence of acute PCH during the postoperative period is 60% among patients undergoing elective craniotomies. No standardized international guidelines are available on the treatment of PCH to the present day. Treatment methods can be different based on the country and institution where they are used, or even physicians individually can have distinct medication regime, which sometimes happens to be habitual and lacks clinical evidences. The Department of Anesthesiology and Intensive Care Medicine at the University of Debrecen has been giving 100 mg diclofenac with analgesic purpose, as part of the premedication to neurosurgical patients for several years. It was observed that the postoperative headache following craniotomy was milder comparing to data published in the international literature. A pilot study was carried out with similar settings which found the that incidence of PCH was lower and less analgesics were required without any further unwanted side-effects among patients who received 100 mg diclofenac as part of the premedication. Hypothesis: 100 mg preoperatively given diclofenac significantly reduces the incidence and severity of postcraniotomy headache.

NCT ID: NCT01894490 Completed - Clinical trials for Postoperative Complications After Gastrointestinal Operations

Randomized Clinical Trial: Nasoenteric Catheter or Jejunostomy

Start date: January 2008
Phase: N/A
Study type: Observational

Curative treatment of upper gastrointestinal tract neoplasms is complex and associated with high morbidity and mortality. In general, the patients are already malnourished, and early postoperative enteral nutrition is recommended. However, there is no consensus concerning the best enteral access route in these cases.

NCT ID: NCT01884298 Completed - Clinical trials for Postoperative Complications

Effect of Different Anesthetic Techniques for Isolated Systolic Hypertensive Patients of Abdominal Surgery on Postoperative Hospital Stay and Morbidity

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

In General anesthesia, two main ways of pain control are used intra-operatively, one is opioids, the other is epidural. Many colleges prefer using epidural analgesia because it is potent and more effective , and also the benefits of stress block, less depression of breath. however, the epidural technique often causes more drop of blood pressure, especially in dehydrated patients. The investigators designed the trial to see if the benefit weigh out the potential risk of epidural in isolated hypertensive patients.

NCT ID: NCT01883752 Completed - Clinical trials for Postoperative Complication

Goal Directed Fluid Management Based on Non-invasive Monitoring

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

The purpose of this study is to evaluate whether goal directed fluid management using respiratory variations in the oxygen saturation by pulse oximetry (SpO2) waveform has potential to decrease postoperative complications and outcomes.