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Postoperative Complications clinical trials

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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.

NCT ID: NCT01389648 Completed - Abdominal Surgery Clinical Trials

Pre-operative Physiotherapy to Prevent Post-operative Complications

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

The purpose of this study is to assess the roll of pre-operative chest physiotherapy, in addition to the usual care given after major abdominal surgery, in the prevention of post-operative respiratory complications.

NCT ID: NCT01378559 Completed - Clinical trials for Postoperative Complications

Patient Satisfaction and Complications With the New Titan® One Touch Release (OTR) Penis Prosthesis

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

The purpose of this study is to assess patient satisfaction with the Titan one touch release penis prosthesis and to register complications with this prosthesis. This will regard the first prostheses inserted at Herlev Hospital/Frederikssund Hospital. Patient satisfaction will be assessed by mailing out the "Erectile Dysfunction Inventory of Treatment Satisfaction (EDITS) Questionnaire" and recording the patient answers. The most important question will be "Overall how satisfied are you with penile prosthesis?". Complications (including infection, bleeding, and mechanical failure) will be assessed by a patient chart review and confirmed by a brief phone interview.