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Surgical Wound clinical trials

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NCT ID: NCT02544061 Completed - Colostomy Stoma Clinical Trials

NM-IL-12 (rHuIL-12) in Subjects With Open Surgical Wounds

Start date: March 1, 2016
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine the safety and tolerability of NM-IL-12 relative to standard of care (SOC; control) in subjects with open surgical wounds.

NCT ID: NCT02505581 Completed - Clinical trials for Surgical Wound Infection

Parenteral Antibiotics Compared to Combination of Oral and Parenteral Antibiotics in Colorectal Surgery Prophylaxis

ORALEV
Start date: May 2015
Phase: Phase 4
Study type: Interventional

Routine antibiotics for the intravenous and oral prophylaxis of colorectal surgery will be used. Experimental group: Patients undergoing elective colorectal surgery that involves, colonic resection. The antibiotic prophylaxis in this group will be composed of: An oral antibiotic pattern of ciprofloxacin (750mg / 12h, 2 doses) and metronidazole (250mg / 8h, 3 doses) the day before surgery. + Control group: Patients undergoing elective colorectal surgery that involves, colonic resection. The antibiotic prophylaxis in this group will be composed of: An intravenous antibiotic pattern of cefuroxime 1g and metronidazole 1,5gr during anesthetic induction. In both groups a second intravenous dose of cefuroxime (750mg) will be administered if the intraoperative time elongates more than three hours or there is an intraoperative bleeding over 1000cc. There won´t be a placebo treatment. Subject compliance will be evaluated according to the usual practice in surgical care field

NCT ID: NCT02459093 Completed - Clinical trials for Surgical Wound Infection

Subcuticular Suture for Cesarean Skin Incision Closure

Start date: May 2015
Phase: Phase 4
Study type: Interventional

A comparison of the type of suture used for cesarean skin incision approximation and the subsequent rate of wound complications has not been widely studied. Investigators seek to compare poliglecaprone 25 and polyglactin 910 suture used in a subcuticular skin closure in Pfannenstiel incisions during cesarean birth and determine the subsequent wound complication rates (SSI, hematoma, seroma, wound separation).

NCT ID: NCT02453165 Completed - Clinical trials for Surgical Wound Dehiscence

Vaginal Cuff Dehiscence Following Total Laparoscopic Hysterectomy: Laparoscopic vs. Transvaginal Cuff Closure

Start date: February 1, 2015
Phase: N/A
Study type: Interventional

Post-hysterectomy vaginal cuff dehiscence is a rare but threatening complication. The investigators will compare transvaginal versus laparoscopic closure of the vaginal vault at the end of a total laparoscopic hysterectomy, in order which of these two modalities of suturing is associated with a lower risk of dehiscence.

NCT ID: NCT02373501 Completed - Clinical trials for Cesarean Wound Repair

Extra - Abdominal Versus Intra - Abdominal Repair of the Uterine Incision at Cesarean Section

EKAM
Start date: January 2013
Phase: N/A
Study type: Interventional

To evaluate the effects of extra-abdominal repair of the uterine incision compared to intra-abdominal repair, and to study is there superiority of one technique over the other in terms of primary outcomes - operative( up to 4 hours after beginning of anesthesia) and post operative ( until day 4 after operation ) measurements , secondary outcomes, long-term outcomes and subjective outcomes. PRIMARY OUTCOMES: Intra - operative ( during the operation up to 4 hours from anesthesia ) - nausea and vomiting - intraoperative hypotension - intraoperative pain Post operative ( 4 hours from anesthesia and until release from hospital ) - Blood transfusion - Venous thromboembolism - Febrile Morbidity - Endometritis - Wound Infection - Death Subjective measures: - complain of pain 1-10 on day 1 post operative - time until walking - number of Days until having bowel movement - overall satisfactory SECONDARY OUTCOMES: - Operative time - Estimated blood loss ( ebl ) - hemoglobin levels - Hospital stay

NCT ID: NCT02348034 Completed - Clinical trials for Surgical Wound Infection

A Randomized Controlled Trial Exploring the Ability of Negative Pressure Wound Therapy (NPWT) to Reduce Colorectal Surgical Site Infections (SSI)

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

The study will explore the ability of negative pressure wound therapy (Prevena dressing) to reduce post operative superficial surgical site infection rate in elective colorectal surgery. Half of the participants will receive Prevena dressing on closed incision immediately after the operation while other half will receive conventional surgical dressing.

NCT ID: NCT02332252 Completed - Clinical trials for Surgical Wound Infection

Electrocautery Versus Scalpel for Surgical Skin Incisions in Cesarean Section.

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

To determine the risk of surgical site infection after surgical skin incision, comparing electrocautery vs. scalpel.

NCT ID: NCT02136004 Completed - Surgical Wound Clinical Trials

The Closer Trial: A Safety and Efficacy Study of the Rex Medical Vascular Sealing System

Closer
Start date: May 2014
Phase: N/A
Study type: Interventional

The objective of this trial is to demonstrate the safety and effectiveness of the Rex Medical Closer Vascular Sealing System in sealing femoral arterial access sites.

NCT ID: NCT02069262 Completed - Surgical Wound Clinical Trials

Angiography Combination Laparoscopy in Patients With Obscure Gastrointestinal Bleeding

Start date: January 2003
Phase: N/A
Study type: Interventional

There were many approaches for patients with obscure gastrointestinal bleeding (OGIB). Capsule endoscopy (CE), double-balloon endoscopy, deep small-bowel spiral enteroscopy, laparoscopy, computed tomography and angiography have been recommended as investigation. However, of these techniques, the evaluation and management of patients with OGIB remains a formidable challenge. We compared the diagnostic yield and long-term outcomes of patients with OGIB randomized to angiogram combination laparoscopy or angiogram alone.

NCT ID: NCT02053948 Completed - Colostomy Clinical Trials

Pursestring Wound Closure vs "Gunsight" Skin Incision and Closure Technique to Reverse Stoma

GSICT1126
Start date: November 30, 2013
Phase: N/A
Study type: Interventional

The use of temporary stomas has been demonstrated to reduce septic complications after colorectal cancer surgery, especially in high-risk anastomosis; therefore, it is necessary to reduce the number of complications secondary to ostomy takedowns, namely wound infection. The aim of this study is to compare the rates of superficial wound infection, healing time and patient satisfaction after pursestring closure vs "gunsight" skin incision and closure technique closure.