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Hernia clinical trials

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NCT ID: NCT01273818 Completed - Inguinal Hernia Clinical Trials

Effectiveness of Topical Antibiotic Prophylaxis in Inguinal Hernia Repair

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

Aim of this study is to measure the effectiveness of topical gentamicin to prevent post-operative infection in inguinal tension-free hernia repair operation.Secondary aim is, if it is effective as a prophylactic agent, to compare it's effect with intra venous single dose cefazolin sodium prophylaxis.

NCT ID: NCT01268514 Completed - Hernia, Abdominal Clinical Trials

ENHANCE: A Prospective EvaluatioN of Permacolâ„¢ in tHe Repair of Complex AbdomiNal Wall CasEs

ENHANCE
Start date: February 2011
Phase:
Study type: Observational

The objective of this prospective study is to evaluate short-term, mid-term, and long-term clinical outcomes associated with the use of Permacolâ„¢ Biological Implant in the treatment of complex abdominal wall defects

NCT ID: NCT01267825 Terminated - Clinical trials for Lumbosacral Radiculopathy

CT Guided Injection for Low Back Radiculopathy: A Randomized Clinical Trial

Start date: September 1, 2010
Phase: Phase 4
Study type: Interventional

Herniated disc sometimes cause back pain radiating down to a leg. This pain can be so severe that it is functionally disabling. The purpose of this randomized clinical trial is to determine if corticosteroid medication, delivered directly to the area near the herniated disc, can improve the pain and functional disability associated with a herniated disc.

NCT ID: NCT01264003 Completed - Inguinal Hernia Clinical Trials

Antibiotic Prophylaxis in Mesh Repair of Inguinal Hernias

Start date: May 2008
Phase: Phase 4
Study type: Interventional

Inguinal hernia repairs is clean surgical procedures. However infection may be a concern when prosthetic materials are used. This prospective randomized study has been set to observe if antibiotic prohylaxis is of benefit in mesh repair of inguinal hernias.

NCT ID: NCT01247389 Completed - Clinical trials for Laparoscopic Colectomy

Incisional Hernia After Midline Versus Transverse Extraction Incision in Laparoscopic Colectomy

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

Incisional hernia (IH) is a common complication of midline laparotomy. Despite the hope that laparoscopic colon resection would result in fewer incisional hernias, prospective studies demonstrate a similar incidence to open surgery. Observational studies suggest that the rate of incisional hernia after laparoscopic colon resection may be reduced with the use of a transverse compared to a midline extraction incision. However, no randomized trails are available, and a midline extraction incision for hemicolectomy remains the standard current approach. The investigators hypothesize that the use of a lower abdominal transverse muscle splitting incision for specimen extraction in laparoscopic colon surgery will result in fewer incisional hernias compared to a midline periumbilical extraction incision.

NCT ID: NCT01243229 Completed - Clinical trials for Congenital Diaphragmatic Hernia

Genetic Analysis of Congenital Diaphragmatic Disorders

Start date: October 2010
Phase:
Study type: Observational

The purpose of this study is to understand the genetic causes of congenital diaphragmatic disorders (CDD), namely congenital diaphragmatic hernia (CDH), eventration and hiatal hernia. Specifically, the investigators plan to: 1. Ascertain informative families and sporadic cases with congenital diaphragmatic disorders and obtain appropriate phenotypic data and genetic material (peripheral blood and/or diaphragm tissue sample). 2. Localize the gene(s) for CDD to specific chromosomal segments using linkage analysis, and determine the role of somatic mutations in CDD. 3. Isolate and characterize genes involved in the pathogenesis of CDD. 4. Develop molecular markers that will facilitate accurate diagnosis (including prenatal diagnosis) and permit correlation of phenotypic variation with specific mutations. 5. Compare RNA-sequencing from tissue samples of children without CDH to those children with CDH.

NCT ID: NCT01240434 Completed - Clinical trials for in Orifices Created by Trocars Measuring =10 mm in Diameter,

Randomized Prospective Trial on the Occurrence of Laparoscopic Trocar Site Hernias

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

The investigators perform a simple-blind randomized trial with two groups, one in which all the orifices are closed by suturing the external fascia of the abdominal wall (Group A), and another in which the orifices are left open, closing only the skin (Group B). Monitoring for trocar site hernia lasted 2 years from the intervention.

NCT ID: NCT01240057 Completed - Clinical trials for Diaphragmatic Hernia

Tracheal Occlusion To Accelerate Lung Growth (TOTAL) Trial for Severe Pulmonary Hypoplasia

TOTAL
Start date: November 2011
Phase: Phase 2/Phase 3
Study type: Interventional

This trial investigates whether prenatal intervention improves survival rate of fetuses with isolated congenital diaphragmatic hernia and severe pulmonary hypoplasia, as compared to expectant management during pregnancy, both followed by standardized postnatal care.

NCT ID: NCT01237470 Terminated - Hernia, Inguinal Clinical Trials

The Desarda and Lichtenstein Techniques in Inguinal Hernia Treatment.

DESLICH
Start date: January 2005
Phase: N/A
Study type: Interventional

Contemporary treatment of inguinal hernia is generally based on surgical methods with the use of synthetic meshes. The implanted meshes however have some disadvantages: they increase the risk of infection, tend to sustain inflammation process, can generate chronic pain and fertility disorders, can move from the initial implantation site, increase costs of treatment etc. The research to find any new hernioplasty without the use of meshes is still going on. Desarda in 2002 year published his own results over hernia treatment with the use of external oblique aponeurosis. These results were comparable with the effects of Lichtenstein technique. The initial assessment done in our own department revealed good clinical results after hernia treatment with Desarda's method. To make appropriate and objective clinical assessment of the Desarda's technique for primary inguinal hernia treatment the randomized multicentre double blinded clinical trial (RCT) was projected and conducted. Finally, 105 patients were included in the Desarda group and 103 in the Lichtenstein group. Personal clinical follow up was made up to 3 years after operation. Generally no statistically significant differences were found between these groups. The only difference was higher rate of seroma after Lichtenstein technique and different pain perception in both groups. To the summary it is clear that Desarda technique is quite attractive and good proposition for operative hernia treatment without mesh. The RCT was done with the use of SharePoint Portal Server (Microsoft) which seems to be appropriate for clinical trials.

NCT ID: NCT01236924 Active, not recruiting - Clinical trials for Lumbar Disc Herniation.

Effectiveness of Global Postural Reeducation in Patients With Chronic Symptomatic Lumbar Disc Herniation

Start date: January 2011
Phase: Phase 1
Study type: Interventional

Slipped disc is the rupture of the fibrous ring, with subsequent displacement of the nucleus pulposus in intervertebral spaces, which may cause compression of nerve structures. It is estimated that 2-3% of the population have taken with this process, whose prevalence is 4.8% in men and 2.5% in women over 35 years. Thus, the purpose of this study is to verify the effectiveness of global postural reeducation in patients diagnosed with chronic symptomatic lumbar disc herniation with the application of a randomized controlled trial. Will be measured pain, disability and functional flexibility.