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Hernia clinical trials

View clinical trials related to Hernia.

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NCT ID: NCT04303442 Completed - Bleeding Clinical Trials

Corona Mortis in Patients Undergoing TEP for Inguinal Hernia

Start date: January 2, 2020
Phase:
Study type: Observational

This study aim to describe the presence, type and size of Corona mortis (CMOR) in patients undergoing total extraperitoneal (TEP) inguinal hernia repair procedures. This study also aim to describe the preperitoneal vascular anatomy of inguinal area and provide in vivo knowledge about CMOR.

NCT ID: NCT04303182 Active, not recruiting - Inguinal Hernia Clinical Trials

LESS TEP vs. Three Port TEP for Inguinal Hernia Repair

Start date: January 2, 2020
Phase: N/A
Study type: Interventional

This study aim to compare efficacy and safety of Laparoendoscopic single site total extraperitoneal inguinal hernia repair /LESS TEP/ and traditional total extraperitoneal hernia repair with 3 ports /TEP/.

NCT ID: NCT04300153 Completed - Postoperative Pain Clinical Trials

The Effect of Erector Spinae Plane Block on Quality of Recovery and Postoperative Analgesia After Inguinal Hernia Repair

Start date: March 25, 2020
Phase: N/A
Study type: Interventional

Inguinal hernia repair (IHR) is one of the most commonly performed operations in general surgery practice. Different pharmacological approaches and interfascial plane blocks are used to control postoperative pain. Erector spinae plane (ESP) block is a relatively new interfascial plane block which was reported to be effective in different types of surgeries. In this study, the primary aim is to assess the effect of ESP on recovery of patients following open IHR surgery.

NCT ID: NCT04295629 Completed - Clinical trials for Ilioinguinal Nerve Block

The Effects of Ilioinguinal Nerve Block on Chronic Pain in Patients in Inguinal Hernia With Spinal Anesthesia

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

Regional anesthesia is a popular anesthetic method in patients who will undergo an inguinal hernia operation. Researchers known that pain in the operating area is a complaint that impairs the quality of life for patients in the long term after the operation. In addition to regional anesthesia, has planned to investigate the effects of applying another drug near the surgery area on pain that may develop in the long term.

NCT ID: NCT04294446 Recruiting - Ventral Hernia Clinical Trials

Post-market Study of the Biodesign Hernia Graft

Start date: November 10, 2020
Phase:
Study type: Observational

The purpose of this study is to collect data on the performance of the Biodesign® Hernia Graft when used to reinforce soft tissues during ventral hernia repair.

NCT ID: NCT04282720 Completed - Hiatal Hernia Clinical Trials

SurgiMend Mesh at the Hiatus

Start date: March 31, 2020
Phase: N/A
Study type: Interventional

Prospective, single-arm, open-label study to evaluate re-occurrence and quality of life in subjects undergoing primary Hiatal hernia repair using SurgiMend biological mesh. Up to 15, with a target of 10, subjects are planned to be enrolled at one site. All subjects will receive the SurgiMend mesh during surgery. Data collected will be compared to historical data. Subjects will complete a pre-operative visit. After surgery, in addition to any standard of care visits, subjects will complete 3- and 6-month follow-ups involving a phone QOL survey and will have an upper GI series at 6 months.

NCT ID: NCT04282473 Recruiting - Parastomal Hernia Clinical Trials

Peristomal Hernia Rate 5 Years After a Terminal Colostomy With the Parietex ™ TCM Parietal Prosthesis Versus Without Mesh

RESEDAE
Start date: May 24, 2022
Phase:
Study type: Observational

This study is a follow-up of the GRECCAR 07 cohort (NCT01380860). Patients will be evaluated 5 years following terminal colostomy to observe patient long-term patient outcomes from colostomy with and without mesh placement.

NCT ID: NCT04280094 Completed - Inguinal Hernia Clinical Trials

Can Ideal Mesh Size be Standardized in Open Inguinal Hernia Repair

Start date: June 2, 2020
Phase:
Study type: Observational

Two hundred consecutive unilateral inguinal hernia patients will be included in the study. Patients will be recorded by measuring the distance between the pubic tubercle and the deep inguinal ring, the distance between the inguinal ligament and the internal oblique aponeurosis, the distance between the deep and superficial inguinal ring diameters and their anterior superior iliac spine. The contribution of these measures to the determination of the ideal mesh size will be analyzed.

NCT ID: NCT04273828 Recruiting - Back Pain Clinical Trials

Impact of Muscle Degeneration in Chronic Low Back Pain

Start date: April 6, 2020
Phase:
Study type: Observational

Surgical interventions for the removal of intervertebral disc fragments or to enlarge a narrow spine canal are commonly performed worldwide and are considered efficient. Concomitant low back pain is not uncommon among patients with lumbar nerve compression and neurological symptoms. When present, controversy persists in the literature regarding its ideal management. Although neurological symptoms improve after decompressive surgery, the presence of residual chronic low back pain may worsen satisfaction scores and cause functional disability. The hypothesis of the present study is that the presence of atrophy of the paraspinal and trunk muscles predicts chronic low back pain after lumbar neural decompression. If confirmed, this finding will aid in better planning of physical rehabilitation strategies for this group of patients, as well as a clearer prediction regarding surgical treatment outcomes for patients and health professionals.

NCT ID: NCT04272320 Completed - Inguinal Hernia Clinical Trials

The Efficacy of Transversalis Fascia Plane Block in Pediatric Inguinal Hernia Repair

Start date: September 29, 2021
Phase: N/A
Study type: Interventional

In patients undergoing lower abdominal surgery, postoperative pain management is frequently provided with systemic opioids use or neuraxial methods. Ultrasound-guided TFP block is the preferred method to reduce the use of opioids and systemic analgesics for postoperative pain management. TFP block provides anesthesia and analgesia in the inguinal region by blocking the ilioinguinal and iliohypogastric nerves. In this study, we aimed to evaluate the effects of ultrasound-guided TFP Block on postoperative pain scores in pediatric lower abdominal surgery.