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Active clinical trials for "Incisional Hernia"

Results 1-10 of 179

The Use of Different Types of Mesh for Prevention of Incisional Hernia Versus Primary Abdominal...

Incisional Hernia

The use of different types of mesh at different sites in prevention of incisional hernia after various abdominal incision versus primary abdominal suturing.

Recruiting8 enrollment criteria

Suture Techniques to Reduce the Incidence of Incisional Hernia: LTFU STITCH Trial

SurgeryIncisional Hernia4 more

Rationale: Incisional hernias (IH) are a frequent complication after abdominal surgery. Prevalence of an IH varies depending on the previous abdominal procedure but could be as high as 70% in high-risk patients after open surgery. To investigate different fascia closure techniques in the prevention of IHs, the STITCH trial (NCT01132209) was designed. The study compared two different closure techniques for closure of a midline incision in adult patients undergoing an elective abdominal laparotomy. Patients were randomly assigned to the intervention group (small bites 5 mm x 5 mm) or the control group (large bites 1 cm x 1 cm). The study showed that small bites are much more effective than large bites in the prevention of an incisional hernia when closing a midline incision. So far, it has not been studied whether there is still a long-term difference in incidence of incisional hernia between the small bites and the large bites group. Objective: The primary objective of this study is to determine the difference in incidence of IH between the small bites and the large bites group after 10 years of follow-up from time of randomization in the STITCH trial. The secondary objectives are to measure quality of life (QoL), body image and cosmetic results, and abdominal wall function through questionnaires and physical examination in those patients who are still alive.

Recruiting5 enrollment criteria

Use of Stratafix Symmetric™ to Prevent Incisional Hernia in Gastrointestinal and Abdominal Surgery...

C.Surgical Procedure; Disruption of WoundSuture

Comparing the use of Stratafix Symmetric™ sutures to standard laparotomy closure sutures.

Recruiting7 enrollment criteria

Suture Repair vs Mesh Repair for Incisional Hernia

Incisional Hernia

The goal of this randomized controlled trial is to compare the difference in quality of life at one year postoperatively for patients undergoing incisional hernia repair with mesh versus suture repair using modern techniques. The main question it aims to answer are: • Determine if primary suture repair is non-inferior to mesh repair for incisional hernias 2-6cm with respect to quality of life using the HerQLes summary score at one year postoperatively.

Recruiting13 enrollment criteria

Optimization of Surgical Treatment of Patients With Incisional Ventral Hernias

Incisional HerniaMedial Hernia1 more

The goal of our work of optimization of the treatment of postoperative hernias is to improve the results of treatment of patients with median and median-lateral postoperative hernias of medium (W2) and large (W3) sizes by developing new surgical techniques. The main questions it aims to answer are: To study the topographic and variant anatomy of vessels and nerves in the retromuscular, preperitoneal, postperitoneal and pre-abdominal cell spaces of the anterior abdominal wall. To determine the most probable sources of blood flow and lymph from the anatomical formations forming the bed of the endoprosthesis. To develop technical, surgical techniques that allow to form an implant bed with minimal traumatization of blood vessels and nerves and reduce the risk of postoperative complications. To develop a technique for plasty of the anterior abdominal wall in mid-lateral postoperative hernias with a combination of retromuscular and subaponeurotic spaces. The researchers will compare an experimental group in which a new method of preparing the implant place will be used and a control group in which standard methods of treating postoperative ventral hernias were used to see whether the new method affects the improvement of the postoperative period and the reduction of complications.

Recruiting2 enrollment criteria

GORE® ENFORM Biomaterial Product Study

HerniaVentral5 more

A prospective, retrospective, non-randomized, multicenter study with two independent hernia study cohorts (Ventral / Incisional Hernia Repair and Diaphragmatic / Hiatal Hernia Repair). The primary objective of this study is to collect GORE® ENFORM Biomaterial product commercial-use data on device functional performance.

Recruiting42 enrollment criteria

Laparoscopic IPOM Plus vs. eTEP Trial

Incisional Hernia of Midline of Abdomen

The survey will compare primary and secondary outcomes of laparoscopic intraperitoneal onlay mesh (IPOM plus) and extended totally extraperitoneal (eTEP) repair for incisional hernia. The research hypothesis is the following: patients who underwent eTEP repair may experience 30% less pain, assessed on the NRS-11 scale by the end of postoperative day 1, compared with IPOM plus procedure

Recruiting12 enrollment criteria

Biosynthetic Absorbable Mesh vs Standard of Repair for the Surgical Treatment of Infected Incisional...

Ventral Hernia Repair

Incisional hernia is one of the most common complications of abdominal surgery and carries a significant burden for both patients and the economic health service. However, no consensus for the surgical treatment of incisional hernia in contaminated field is currently available. The purpose of the COMpACT-BIO study is to investigate the clinical and economic benefit of the use of biosynthetic mesh in contaminated incisional hernia repair.

Recruiting16 enrollment criteria

RCT Ventralex vs Onlay Mesh in Incisional Hernias

Incisional Hernia of Midline of Abdomen

A radomised controlled trial comparing Ventralex patch and Progrip mesh in surgery for midline incisional hernias

Recruiting8 enrollment criteria

Incisional Hernia in Infants and Children

Incisional Hernia

the study of development of incisional hernia in infants and children at a tertiary level experience.

Recruiting2 enrollment criteria
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