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Incisional Hernia clinical trials

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NCT ID: NCT04801394 Completed - Incisional Hernia Clinical Trials

Retrospective Analysis on Large Incisional Hernia in High Risk Patients

Start date: April 1, 2010
Phase: N/A
Study type: Interventional

Large incisional hernia (LIH) is a challenging condition where the abdominal wall is hopelessly compromised. Nowadays the best treatment option in this particularly frail subset of patients is a major issue. The Auhtors proposed the clinical experience with an innovative approach with the composite Free Lateral Polypropylene prosthesis (FLaPp®) mesh fashioned as "neoperitoneum" analyzing its feasibility and short/medium term results.

NCT ID: NCT04700956 Completed - Incisional Hernia Clinical Trials

Does the Use of Prophylactic Mesh Reduce Incisional Hernia?

Start date: December 19, 2020
Phase: N/A
Study type: Interventional

Incisional hernia is a common condition after abdominal surgery. Because linea alba has less vascularity, incisional hernia more common in midline incisions. It is seen in the general population between 11-20%. In some high-risk situations, this rate increases up to 40-69% (abdominal aortic aneurysm, morbid obesity, colorectal surgery).It is known that incisional hernia that occurs in the postoperative period can lead to emergency surgical causes such as incarceration-strangulation, has a significant share in health expenses and seriously impairs the quality of life in patients.One of the methods tried to reduce incisional hernia is the use of mesh. But this abdominal closure technique is not used routinely in our country and the other countries. This study will be important of the studies in Turkey and world for patient selection in prophylactic mesh use, techniques to be applied and early / late results. The aim of the study is to compare the classical abdominal closure technique with use of mesh in order to minimize the incisional hernia and associated complications after midline laparotomy.

NCT ID: NCT04578561 Completed - Clinical trials for Prevention of Incisional Hernia in Emergency Surgery

Long-term Follow-up of Prophylactic Mesh Reinforcement After Emergency Laparotomy.

Start date: January 2010
Phase:
Study type: Observational

Observational Study analyzing the long-term results of prophylactic mesh used for preventing incisional hernia after emergency midline laparotomies.

NCT ID: NCT04436887 Completed - Wound Infection Clinical Trials

Prophylactic Sub-lay Non-absorbable Mesh Following Midline Laparotomy: PROMETHEUS (PROphylactic Mesh Trial Evaluation UltraSound)

PROMETHEUS
Start date: January 1, 2016
Phase: N/A
Study type: Interventional

The aim of the present study is to analyse feasibility, safety and Incisional Hernia rate using a prophylactic sub lay non-absorbable mesh [Parietex Progrip (Medtronic) ] in order to prevent Incisional Hernia following midline emergent laparotomy in clean and clean-contaminated wounds.

NCT ID: NCT04434573 Completed - Clinical trials for Study of Practices of Surgeons on Surgical Management of Asymptomatic Hernias

Consensus in Surgical Community for Asymptomatic Abdominal Wall and Incisional Hernias

Start date: October 2016
Phase:
Study type: Observational

Hernia pathology is one of the leading causes of surgery worldwide. For asymptomatic patients, surgery remains questionable. Although there are new European recommendations, the practice of digestive surgeons regarding the management of asymptomatic hernias is unknown. The objective of this study was to evaluate the practices of a large population of digestive surgeons with asymptomatic hernia.

NCT ID: NCT04430816 Completed - Clinical trials for Hernia Incisional Ventral

Management Of Large Incisional Hernia, Double Mesh Modification Of Chevrel's Technique Versus On Lay Mesh Hernioplasty

Start date: January 1, 2017
Phase: N/A
Study type: Interventional

comparison between two groups of large midline incisional hernia, the first group managed by double mesh modification of chevrel's technique the second one managed by conventional onlay mesh repair

NCT ID: NCT04410744 Completed - Incisional Hernia Clinical Trials

Incidence and Risk Factors for TSIH

TSIHi
Start date: June 2, 2015
Phase:
Study type: Observational

Trocar site incisional hernia (TSIH) is the most frequent complication associated to laparoscopic surgery. Few studies currently describes its real prevalence or risk factors. The aim of this study is to determine the real incidence of TSIH and to identify risk factors in the investigator's series of patients. A cross sectional, prospective study is performed including consecutive patients who underwent a laparoscopic procedure during a four months period. All the patients are assessed both clinically (TSIHc) and by an ultrasonographic exam (TSIHu). Main variable studied is the incidence of TSIH. A multivariate analysis is performed to identify risk factors.

NCT ID: NCT04394988 Completed - Incisional Hernia Clinical Trials

Total 102 Natural Orifice Specimen Extractions Following Laparoscopic Colorectal Resections

Start date: January 1, 2013
Phase:
Study type: Observational

In the development of surgical technique, laparoscopic surgery has created a major breaking point. Although laparoscopy (decreased hospital stay, decreased incisional hernia and wound infection rateā€¦) provides a remarkable advantage compared to open surgery, the need for the extraction site incision could not bring the incision-related morbidity rates to the desired level. That's why SILS and natural hole surgery came to the fore. Colorectal surgery was also affected by this process, and the laparoscopic colectomy procedure combined with transrectal colon extraction was first performed in 1993 (1). Although its use increased gradually after this period, it could not reach the expected levels and this could not resolve the concerns on natural hole surgery. In this article, our aim is to present the single center results of the patients who performed the extraction with the NOSE method after laparoscopic colorectal surgery.

NCT ID: NCT04254237 Completed - Incisional Hernia Clinical Trials

Trocar Site Hernia After Laparoscopic Cholecystectomy, Supra Versus Infraumbilical Incision for Umbilical Trocar Entry

HOT
Start date: February 6, 2020
Phase: N/A
Study type: Interventional

Trocar site hernia is a specific complication of laparoscopic surgery. The increasingly frequent use of the laparoscopic approach has resulted in an increase in the number of hernias, mainly at the umbilical area. The appearance of a trocar site hernia can cause complications in the short and long term to the patient who may end up needing a reoperation. In this study we want to compare the supraumbilical versus the infraumbilical location of the laparoscopy entry trocar, in terms of incisional hernia incidence.

NCT ID: NCT04222517 Completed - Hernia, Ventral Clinical Trials

The Use of Local Hemostatic in Patients With Large Incisional Hernias

Start date: September 10, 2017
Phase: N/A
Study type: Interventional

Design of a simple blind randomized controlled trial study. Large incisional hernia repair with use of local hemostatic Hemoblock