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Wound Infection clinical trials

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NCT ID: NCT01408745 Terminated - Clinical trials for Sternum Wound Infection

Sternal Closure With STERNUMFIX in Patients With High Risk

STEPHIX
Start date: June 2008
Phase: Phase 4
Study type: Interventional

The primary objective is to establish if the SternumFix System improves sternal closure. The study should test the hypothesis that in a high risk patient population with increased risk for the development of sternal wound complications SternumFix will reduce the incidence of sternal healing complications. The control group will be treated with wire cerclage, the standard method of sternal closure.

NCT ID: NCT01169064 Terminated - Wound Infection Clinical Trials

Topical Silver for Prevention of Wound Infection After Cesarean Delivery

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

A common concern in any surgical procedure is the occurrence of infection. Silver-containing treatments are popular and used in wound treatment; however, there is presently little evidence of the effectiveness of silver-containing treatment for the prevention of obstetrical wound infection. We plan to investigate the rate of infection in women experiencing cesarean sections at VUMC by comparing the infection rate based on a randomized choice of silver-containing wound dressings to soft cloth adhesive wound dressings.

NCT ID: NCT01133600 Terminated - Diabetic Foot Clinical Trials

Outpatient Treatment of Gram Positive Wound Infections in the Diabetic Foot: A Pharmaco-economic Comparison of Daptomycin vs. Vancomycin Based Regimens

Start date: August 2010
Phase: Phase 4
Study type: Interventional

The purpose of the study is to evaluate the overall burden to the participant (economic, quality of life, patients satisfaction and freedom from side effects) when treating Gram positive infections of the foot in diabetic adults with daptomycin versus vancomycin.

NCT ID: NCT00654641 Terminated - Wound Infection Clinical Trials

Prevention of Wound Complications After Cesarean Delivery in Obese Women Utilizing Negative Pressure Wound Therapy

Start date: September 2007
Phase: N/A
Study type: Interventional

Wound complications after Cesarean section (C-section) are common in obese women. Approximately 25% of obese women having a C-section will have a wound complication. This research study is designed to assess whether applying a source of vacuum (suction) to the wound can reduce the risk of wound complications. The investigators plan to enroll 220 women into the study. Women will be randomly selected to receive standard stitching and stapling of the incision (cut on the abdomen) or closure with stitches, staples and wound suction. Subjects will be seen for follow-up visits in 7-14 days and again at 4-6 weeks after surgery. The number of wound complications in each group will be compared. If the wound suction technique is successful in preventing wound complications, this may substantially reduce pain and suffering in a large number of women undergoing C-section for delivery.

NCT ID: NCT00651131 Terminated - Wound Infections Clinical Trials

Cubicin(R) for Complicated Post-surgical Wound Infections

PSW
Start date: June 1, 2004
Phase: Phase 4
Study type: Interventional

The purpose of the study is to describe the clinical efficacy of CUBICIN therapy in patients with superficial and deep post-surgical Gram-positive wound infections

NCT ID: NCT00528008 Terminated - Wound Infection Clinical Trials

A Comparison of Surgical Preparations and Wound Infection Rates for Elective Cesarean Sections

Start date: December 2007
Phase: Phase 3
Study type: Interventional

The purpose of this study is to find out if chlorhexidine gluconate solution is better at reducing the rate of wound infection after cesarean section compared to povidone-iodine.

NCT ID: NCT00500669 Terminated - Recurrence Clinical Trials

A Randomised Study to Assess Betadine in the Groin Wound of Patients Undergoing Primary Varicose Vein Surgery

Start date: June 2004
Phase: Phase 3
Study type: Interventional

To investigate whether Betadine can reduce infection rates and recurrence rates following varicose veins surgery in a randomized double blind placebo controlled study.

NCT ID: NCT00386477 Terminated - Cesarean Section Clinical Trials

Vaginal Cleansing at Cesarean Delivery to Reduce Infection: A Randomized, Controlled Trial

Start date: September 2006
Phase: N/A
Study type: Interventional

The objective of the project is to find out whether cleansing the vagina before a cesarean delivery decreases the risk of complications and infections after having the baby. If this is the case, cleansing the vagina before cesarean delivery can help improve outcomes for many women and make their early postpartum recovery much more pleasant, giving a healthier start for the family.

NCT ID: NCT00315822 Terminated - Clinical trials for Surgical Wound Infection

Supplemental Postoperative Oxygen and Wound Infection in Morbidly Obese Patients

Start date: May 2006
Phase: Phase 3
Study type: Interventional

The investigators propose to test the hypothesis that the incidence of major complications related to infection or inadequate healing is reduced in morbidly obese patients given 80% inspired oxygen during, and for 12-18 hours after, surgery compared with patients given 80% oxygen only during surgery. The primary outcome will be a composite of major complications plausibly related to infection or healing.

NCT ID: NCT00260494 Terminated - Clinical trials for Postoperative Complications

Acupuncture and Post-Surgical Wound Healing

Start date: March 2005
Phase: N/A
Study type: Interventional

The purpose of this study is to determine if acupuncture improves wound healing. Since we, the investigators at the University of California, San Francisco (UCSF), know that how much oxygen is delivered to tissue is the best predictor of how well a wound will heal, we are measuring changes in tissue oxygen of wounds before and after acupuncture treatments. We are focusing on the leg wounds of coronary artery bypass graft (CABG) patients who have their saphenous veins harvested in an open fashion since this is a fairly well controlled patient model.