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Hernia clinical trials

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NCT ID: NCT01282606 Completed - Clinical trials for Lumbar Vertebra Hernia

Clinical Trial to Assess Safety of SI-6603 in Patients With Lumbar Disc Herniation

Start date: December 2007
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate the safety of SI-6603 in lumbar disc herniation patients.

NCT ID: NCT01280370 Completed - Clinical trials for Incisional Hernia Repair

Prospective Evaluation of Laparoscopic and Open Incisional Hernia Repair: a Multicenter Cohort Study

IHR_SALTC
Start date: September 2010
Phase:
Study type: Observational

Nowadays incisional hernia are primarily repaired using prosthetic meshes. In Switzerland such meshes are mainly implanted via open or laparoscopic approach. The differential impact of these two types of surgical technique on recurrence rate will be investigated with this study. With this multicenter cohort study the outcomes of laparoscopic and open incisional hernia repair will be investigated prospectively. Hernia recurrence is the main outcome measure. Hypothesis: Laparoscopic incisional hernia repair is associated with a lower recurrence rate compared to open incisional hernia repair.

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: 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: NCT01224145 Completed - Postoperative Pain Clinical Trials

Assess the Feasibility and Efficacy of the CollaRx® Bupivacaine Implant Laparoscopic Inguinal or Umbilical Herniorrhaphy

Start date: March 22, 2011
Phase: Phase 2
Study type: Interventional

This study will assess pain intensity for the first 72 hrs after aggravated movement (cough) following Laparoscopic Inguinal or Umbilical Herniorrhaphy.