Clinical Trials Logo

Hernia clinical trials

View clinical trials related to Hernia.

Filter by:

NCT ID: NCT04450628 Recruiting - Hiatal Hernia Clinical Trials

Esophagogastric Junction Distensibility During Hiatal Hernia Repair

Start date: September 28, 2020
Phase: N/A
Study type: Interventional

The investigators aim to ascertain the effects of hiatal hernia repair and fundoplication on the distensibility of the esophagogastric junction (EGJ) as measured by FLIP topography/impedance planimetry. The investigators also aim to assess for any correlation between values of EGJ distensibility and GERD related quality of life (QOL) and dysphagia scores.

NCT ID: NCT04440514 Recruiting - Parastomal Hernia Clinical Trials

Endoscopic Preperitoneal Parastomal Hernia Repair (ePauli Repair)

ePauli
Start date: June 1, 2020
Phase:
Study type: Observational [Patient Registry]

Observational study on laparoscopic and robotic extraperitoneal mesh repair of parastomal hernia, employing TAR.

NCT ID: NCT04438369 Completed - Postoperative Pain Clinical Trials

Evaluation of Ultrasound-guided Erector Spinae Block for Postoperative Analgesia in Laprascopic Ventral Hernia Repair.

Start date: September 1, 2020
Phase: N/A
Study type: Interventional

Ventral hernia repair is associated with significant postoperative pain, and regional anesthetic techniques are of potential benefit. The postoperative mobility and training is of utmost importance in this patient group, and could be increased using local anesthetics instead of opioids. Inadequate post-operative pain control can lead to adverse consequences for patients, such as the development of chronic pain, immunosuppression, poorer healing of surgical wounds, as well as adrenergic activation and its consequences in the form of coronary incidents or gastrointestinal obstruction and postoperative nausea and vomiting (PONV). Moreover, lack of mobility can result in thrombosis and embolism. These complications affect hospital functioning, which leads to decreased patient satisfaction, a worse reputation for the hospital, longer stays in the recovery room, prolonged hospitalizations, higher incidence of re-surgeries and re-admissions, and higher costs for care and treatment. Erector spinae plane block (ESPB) is the latest of the truncal blocks and was first described in 2016. The efficacy of bilateral ESPB at the T7 level has been described in a study of 4 cases, moreover effective analgesia with ESPB after bariatric surgery has been described in a study of 3 cases. When performed at the level of the T7 transverse process, studies show the potential to block both supra-umbilical and infra-umbilical dermatomes. So far there are mostly case studies done in this field of study, and internationally there is a call for research into the effect of this technique and randomized controlled trials. The objective of this study is to compare ESPB to multimodal analgesia in patients undergoing ventral hernia repair.

NCT ID: NCT04437784 Completed - Clinical trials for Bilateral Inguinal Hernia

Laparoscopic Versus Open Mesh Repair of Bilateral Primary Inguinal Hernia

Start date: June 2014
Phase: N/A
Study type: Interventional

The best approach for simultaneous repair of bilateral inguinal hernia is controversial. The aim of this study is to compare the outcomes after laparoscopic versus open mesh repair of bilateral primary inguinal hernia

NCT ID: NCT04437043 Active, not recruiting - Ventral Hernia Clinical Trials

A Multicenter Belgian Trial of Ventral Hernia Repair

UNITE
Start date: December 16, 2020
Phase: N/A
Study type: Interventional

Patients with incisional midline ventral hernias with a minimal width of 3 cm and a maximal width of 8 cm, treated according to the standard practice of the participating investigators. Patients can be treated with the following ventral hernia repair approaches: - Laparoscopic ventral hernia repair with closure of the defect (IPOM+) - Open ventral hernia repair with closure of the defect (retromuscular repair) - Robotic ventral hernia repair with closure of the defect (retromuscular repair) To evaluate the total number of days spent in the hospital within a period of 90 days post-operative. This will be calculated by adding the hospital length of stay for initial surgery or index-procedure, length of stay for any additional readmission resulting from the surgery or re-interventions, and emergency room visits resulting from the surgery or Serious Adverse Event (SAE) related to the index-procedure. Secondary objectives: To assess the safety, performance and efficacy of laparoscopic, open and robotic ventral hernia repair.

NCT ID: NCT04436159 Completed - Clinical trials for Gastro Esophageal Reflux

Partial Versus Total Fundoplication in the Surgical Repair of Para-esophageal Hernia.

Start date: May 1, 2009
Phase: N/A
Study type: Interventional

Short-term follow up after surgery of para-esophageal hernia comparing two different types of fundoplication

NCT ID: NCT04435340 Completed - Abdominal Hernia Clinical Trials

Ventral Abdominal Hernia Repair With Self Adhering, Atraumatic Mesh

Start date: March 22, 2018
Phase: N/A
Study type: Interventional

Patients who underwent ventral abdominal hernia repair with self adhering, atraumatic mesh in sublay position are examined for their recurrence rate

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: NCT04434378 Terminated - Clinical trials for Post Operative Urinary Retention

Tamsulosin to Prevent Postoperative Urinary Retention in Laparoscopic Inguinal Hernia Repair

Start date: November 16, 2017
Phase: Phase 4
Study type: Interventional

To investigate the effect of tamsulosin on the development of post-operative urinary retention (PUR) after elective laparoscopic inguinal hernia repair (LIHR). This will be accomplished by administering a pre-operative dose of tamsulosin. The primary outcome is the rate of urinary retention necessitating straight catheterization or insertion of foley catheter prior to discharge.

NCT ID: NCT04431271 Completed - Inguinal Hernia Clinical Trials

Economic Assessment of STarting Endoscopic Robotic Groin Hernia Repair

EASTER
Start date: June 1, 2020
Phase:
Study type: Observational

The material cost for robotic groin hernia repair is higher than for conventional laparoscopic surgery. In this study, this amount will be quantified and possible differences in early postoperative course, hospital stay and readmission rate that could influence the cost/benefit ratio for robotic groin hernia surgery will be analyzed.